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nsv5468832

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:39,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 377 SVs from 68 studies. See in: genome view    
Submitted genomic68,813,000-68,852,000Question Mark
Overlapping variant regions from other studies: 377 SVs from 68 studies. See in: genome view    
Remapped(Score: Perfect):69,678,718-69,717,718Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5468832Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr468,813,00068,852,000
nsv5468832RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr469,678,71869,717,718

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16950544duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16950544Submitted genomicNC_000004.12:g.688
13000_68852000dup
GRCh38 (hg38)NC_000004.12Chr468,813,00068,852,000
nssv16950544RemappedPerfectNC_000004.11:g.696
78718_69717718dup
GRCh37.p13First PassNC_000004.11Chr469,678,71869,717,718

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)
nssv169505440.008506404
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