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nsv5507012

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:888

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 107 SVs from 26 studies. See in: genome view    
Submitted genomic40,725,899-40,726,786Question Mark
Overlapping variant regions from other studies: 107 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):41,018,097-41,018,984Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5507012Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1540,725,89940,726,786
nsv5507012RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1541,018,09741,018,984

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17700133deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17700133Submitted genomicNC_000015.10:g.407
25899_40726786del
GRCh38 (hg38)NC_000015.10Chr1540,725,89940,726,786
nssv17700133RemappedPerfectNC_000015.9:g.4101
8097_41018984del
GRCh37.p13First PassNC_000015.9Chr1541,018,09741,018,984

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)
nssv17700133<0.00116404
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