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nsv5496925

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:98

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 97 SVs from 17 studies. See in: genome view    
Submitted genomic58,439,487-58,439,584Question Mark
Overlapping variant regions from other studies: 97 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):58,906,205-58,906,302Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5496925Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1458,439,48758,439,584
nsv5496925RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1458,906,20558,906,302

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17695881duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17695881Submitted genomicNC_000014.9:g.5843
9487_58439584dup
GRCh38 (hg38)NC_000014.9Chr1458,439,48758,439,584
nssv17695881RemappedPerfectNC_000014.8:g.5890
6205_58906302dup
GRCh37.p13First PassNC_000014.8Chr1458,906,20558,906,302

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)
nssv17695881<0.00116404
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