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esv2577003

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,162

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 437 SVs from 59 studies. See in: genome view    
Remapped(Score: Perfect):152,399,521-152,402,682Question Mark
Overlapping variant regions from other studies: 439 SVs from 59 studies. See in: genome view    
Remapped(Score: Perfect):152,096,606-152,099,767Question Mark
Overlapping variant regions from other studies: 169 SVs from 17 studies. See in: genome view    
Submitted genomic151,727,539-151,730,700Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2577003RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7152,399,521152,402,682
esv2577003RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7152,096,606152,099,767
esv2577003Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000007.12Chr7151,727,539151,730,700

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv5181593copy number gainNA18507SequencingRead depth232,775

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv5181593RemappedPerfectNC_000007.14:g.(?_
152399521)_(152402
682_?)dup
GRCh38.p12First PassNC_000007.14Chr7152,399,521152,402,682
essv5181593RemappedPerfectNC_000007.13:g.(?_
152096606)_(152099
767_?)dup
GRCh37.p13First PassNC_000007.13Chr7152,096,606152,099,767
essv5181593Submitted genomicNC_000007.12:g.(?_
151727539)_(151730
700_?)dup
NCBI36 (hg18)NC_000007.12Chr7151,727,539151,730,700

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

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