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nsv5530125

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:37,449

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 225 SVs from 44 studies. See in: genome view    
Submitted genomic10,710,688-10,748,136Question Mark
Overlapping variant regions from other studies: 225 SVs from 44 studies. See in: genome view    
Remapped(Score: Perfect):10,614,005-10,651,453Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5530125Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1710,710,68810,748,136
nsv5530125RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1710,614,00510,651,453

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17711401deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17711401Submitted genomicNC_000017.11:g.107
10688_10748136del
GRCh38 (hg38)NC_000017.11Chr1710,710,68810,748,136
nssv17711401RemappedPerfectNC_000017.10:g.106
14005_10651453del
GRCh37.p13First PassNC_000017.10Chr1710,614,00510,651,453

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17711401<0.00116404
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