U.S. flag

An official website of the United States government

esv2763779

  • Variant Calls:7
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:32,835

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 488 SVs from 56 studies. See in: genome view    
Remapped(Score: Perfect):8,783,681-8,816,515Question Mark
Overlapping variant regions from other studies: 488 SVs from 56 studies. See in: genome view    
Remapped(Score: Perfect):8,825,367-8,858,201Question Mark
Overlapping variant regions from other studies: 208 SVs from 20 studies. See in: genome view    
Submitted genomic8,800,367-8,833,201Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartOuter Stop
esv2763779RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr38,783,6818,816,515
esv2763779RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr38,825,3678,858,201
esv2763779Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000003.10Chr38,800,3678,833,201

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv7026144copy number gainSW_0183SNP arraySNP genotyping analysis45
essv7026155copy number gainSW_0628SNP arraySNP genotyping analysis42
essv7026166copy number gainSW_0659SNP arraySNP genotyping analysis35
essv7026177copy number gainSW_0791SNP arraySNP genotyping analysis38
essv7026189copy number gainSW_1309SNP arraySNP genotyping analysis40
essv7026200copy number gainSW_1337SNP arraySNP genotyping analysis23
essv7026211copy number gainSW_1423SNP arraySNP genotyping analysis33

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv7026144RemappedPerfectNC_000003.12:g.(?_
8783681)_(8816515_
?)dup
GRCh38.p12First PassNC_000003.12Chr38,783,6818,816,515
essv7026155RemappedPerfectNC_000003.12:g.(?_
8783681)_(8816515_
?)dup
GRCh38.p12First PassNC_000003.12Chr38,783,6818,816,515
essv7026166RemappedPerfectNC_000003.12:g.(?_
8783681)_(8816515_
?)dup
GRCh38.p12First PassNC_000003.12Chr38,783,6818,816,515
essv7026177RemappedPerfectNC_000003.12:g.(?_
8783681)_(8816515_
?)dup
GRCh38.p12First PassNC_000003.12Chr38,783,6818,816,515
essv7026189RemappedPerfectNC_000003.12:g.(?_
8783681)_(8816515_
?)dup
GRCh38.p12First PassNC_000003.12Chr38,783,6818,816,515
essv7026200RemappedPerfectNC_000003.12:g.(?_
8783681)_(8816515_
?)dup
GRCh38.p12First PassNC_000003.12Chr38,783,6818,816,515
essv7026211RemappedPerfectNC_000003.12:g.(?_
8784222)_(8816515_
?)dup
GRCh38.p12First PassNC_000003.12Chr38,784,2228,816,515
essv7026144RemappedPerfectNC_000003.11:g.(?_
8825367)_(8858201_
?)dup
GRCh37.p13First PassNC_000003.11Chr38,825,3678,858,201
essv7026155RemappedPerfectNC_000003.11:g.(?_
8825367)_(8858201_
?)dup
GRCh37.p13First PassNC_000003.11Chr38,825,3678,858,201
essv7026166RemappedPerfectNC_000003.11:g.(?_
8825367)_(8858201_
?)dup
GRCh37.p13First PassNC_000003.11Chr38,825,3678,858,201
essv7026177RemappedPerfectNC_000003.11:g.(?_
8825367)_(8858201_
?)dup
GRCh37.p13First PassNC_000003.11Chr38,825,3678,858,201
essv7026189RemappedPerfectNC_000003.11:g.(?_
8825367)_(8858201_
?)dup
GRCh37.p13First PassNC_000003.11Chr38,825,3678,858,201
essv7026200RemappedPerfectNC_000003.11:g.(?_
8825367)_(8858201_
?)dup
GRCh37.p13First PassNC_000003.11Chr38,825,3678,858,201
essv7026211RemappedPerfectNC_000003.11:g.(?_
8825908)_(8858201_
?)dup
GRCh37.p13First PassNC_000003.11Chr38,825,9088,858,201
essv7026144Submitted genomicNC_000003.10:g.(?_
8800367)_(8833201_
?)dup
NCBI36 (hg18)NC_000003.10Chr38,800,3678,833,201
essv7026155Submitted genomicNC_000003.10:g.(?_
8800367)_(8833201_
?)dup
NCBI36 (hg18)NC_000003.10Chr38,800,3678,833,201
essv7026166Submitted genomicNC_000003.10:g.(?_
8800367)_(8833201_
?)dup
NCBI36 (hg18)NC_000003.10Chr38,800,3678,833,201
essv7026177Submitted genomicNC_000003.10:g.(?_
8800367)_(8833201_
?)dup
NCBI36 (hg18)NC_000003.10Chr38,800,3678,833,201
essv7026189Submitted genomicNC_000003.10:g.(?_
8800367)_(8833201_
?)dup
NCBI36 (hg18)NC_000003.10Chr38,800,3678,833,201
essv7026200Submitted genomicNC_000003.10:g.(?_
8800367)_(8833201_
?)dup
NCBI36 (hg18)NC_000003.10Chr38,800,3678,833,201
essv7026211Submitted genomicNC_000003.10:g.(?_
8800908)_(8833201_
?)dup
NCBI36 (hg18)NC_000003.10Chr38,800,9088,833,201

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

Support Center