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nsv5494929

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:272,429

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 889 SVs from 73 studies. See in: genome view    
Submitted genomic45,956,758-46,229,186Question Mark
Overlapping variant regions from other studies: 889 SVs from 73 studies. See in: genome view    
Remapped(Score: Perfect):46,425,961-46,698,389Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5494929Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1445,956,75846,229,186
nsv5494929RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1446,425,96146,698,389

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17694674deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17694674Submitted genomicNC_000014.9:g.4595
6758_46229186del
GRCh38 (hg38)NC_000014.9Chr1445,956,75846,229,186
nssv17694674RemappedPerfectNC_000014.8:g.4642
5961_46698389del
GRCh37.p13First PassNC_000014.8Chr1446,425,96146,698,389

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)
nssv17694674<0.00116404
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