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nsv5525141

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:56,763

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 333 SVs from 57 studies. See in: genome view    
Submitted genomic56,626,482-56,683,244Question Mark
Overlapping variant regions from other studies: 333 SVs from 57 studies. See in: genome view    
Remapped(Score: Perfect):56,660,394-56,717,156Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5525141Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1656,626,48256,683,244
nsv5525141RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1656,660,39456,717,156

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17709427duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17709427Submitted genomicNC_000016.10:g.566
26482_56683244dup
GRCh38 (hg38)NC_000016.10Chr1656,626,48256,683,244
nssv17709427RemappedPerfectNC_000016.9:g.5666
0394_56717156dup
GRCh37.p13First PassNC_000016.9Chr1656,660,39456,717,156

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)
nssv17709427<0.00126404
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