U.S. flag

An official website of the United States government

esv1838633

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:798,202

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2904 SVs from 101 studies. See in: genome view    
Remapped(Score: Pass):61,578,038-62,376,239Question Mark
Overlapping variant regions from other studies: 1221 SVs from 85 studies. See in: genome view    
Remapped(Score: Pass):62,180,400-62,294,432Question Mark
Overlapping variant regions from other studies: 2268 SVs from 95 studies. See in: genome view    
Remapped(Score: Pass):62,308,236-62,513,723Question Mark
Overlapping variant regions from other studies: 61 SVs from 14 studies. See in: genome view    
Remapped(Score: Pass):334,948-610,813Question Mark
Overlapping variant regions from other studies: 2811 SVs from 98 studies. See in: genome view    
Remapped(Score: Perfect):61,752,487-61,974,101Question Mark
Overlapping variant regions from other studies: 1231 SVs from 27 studies. See in: genome view    
Submitted genomic61,389,922-61,611,536Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner Stop
esv1838633RemappedPassGRCh38.p12Primary AssemblySecond PassNC_000007.14Chr7-61,578,03862,376,239
esv1838633RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7-62,180,40062,294,432
esv1838633RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr762,308,23662,308,23662,513,723
esv1838633RemappedPassGRCh38.p12Primary AssemblySecond PassNT_187383.1Chr16|NT_1
87383.1		-334,948610,813
esv1838633RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr761,752,48761,752,48761,974,101
esv1838633Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000007.12Chr761,389,92261,396,07861,611,536

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv4387935copy number gainNA10851SNP arraySNP genotyping analysis9,157

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner Stop
essv4387935RemappedPassNC_000007.14:g.(?_
61578038)_(6237623
9_?)dupNC_000007.1
4:g.(62308236_6230
8236)_(62513723_?)
dupNT_187383.1:g.(
?_334948)_(610813_
?)dupNC_000007.14:
g.(?_62180400)_(62
294432_?)dup		GRCh38.p12Second PassNC_000007.14Chr7-61,578,03862,376,239
essv4387935RemappedPassNC_000007.14:g.(?_
61578038)_(6237623
9_?)dupNC_000007.1
4:g.(62308236_6230
8236)_(62513723_?)
dupNT_187383.1:g.(
?_334948)_(610813_
?)dupNC_000007.14:
g.(?_62180400)_(62
294432_?)dup		GRCh38.p12First PassNC_000007.14Chr7-62,180,40062,294,432
essv4387935RemappedPassNC_000007.14:g.(?_
61578038)_(6237623
9_?)dupNC_000007.1
4:g.(62308236_6230
8236)_(62513723_?)
dupNT_187383.1:g.(
?_334948)_(610813_
?)dupNC_000007.14:
g.(?_62180400)_(62
294432_?)dup		GRCh38.p12First PassNC_000007.14Chr762,308,23662,308,23662,513,723
essv4387935RemappedPassNC_000007.14:g.(?_
61578038)_(6237623
9_?)dupNC_000007.1
4:g.(62308236_6230
8236)_(62513723_?)
dupNT_187383.1:g.(
?_334948)_(610813_
?)dupNC_000007.14:
g.(?_62180400)_(62
294432_?)dup		GRCh38.p12Second PassNT_187383.1Chr16|NT_1
87383.1		-334,948610,813
essv4387935RemappedPerfectNC_000007.13:g.(61
752487_61752487)_(
61974101_?)dup		GRCh37.p13First PassNC_000007.13Chr761,752,48761,752,48761,974,101
essv4387935Submitted genomicNC_000007.12:g.(61
389922_61396078)_(
61611536_?)dup		NCBI36 (hg18)NC_000007.12Chr761,389,92261,396,07861,611,536

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

You are here: NCBI
Support Center