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nsv5627612

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 125 SVs from 32 studies. See in: genome view    
Submitted genomic107,591,641-107,591,641Question Mark
Overlapping variant regions from other studies: 125 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):107,232,086-107,232,086Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5627612Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7107,591,641107,591,641
nsv5627612RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7107,232,086107,232,086

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv17156155insertionHG03486SequencingSequence alignment4,355

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17156155Submitted genomicNC_000007.14:g.107
591641_107591642in
s51
GRCh38 (hg38)NC_000007.14Chr7107,591,641107,591,641
nssv17156155RemappedPerfectNC_000007.13:g.107
232086_107232087in
s51
GRCh37.p13First PassNC_000007.13Chr7107,232,086107,232,086

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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