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nsv5468408

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:24,599

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 252 SVs from 58 studies. See in: genome view    
Submitted genomic119,303,930-119,328,528Question Mark
Overlapping variant regions from other studies: 252 SVs from 58 studies. See in: genome view    
Remapped(Score: Perfect):120,225,085-120,249,683Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5468408Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4119,303,930119,328,528
nsv5468408RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4120,225,085120,249,683

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16954156duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16954156Submitted genomicNC_000004.12:g.119
303930_119328528du
p
GRCh38 (hg38)NC_000004.12Chr4119,303,930119,328,528
nssv16954156RemappedPerfectNC_000004.11:g.120
225085_120249683du
p
GRCh37.p13First PassNC_000004.11Chr4120,225,085120,249,683

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)
nssv16954156<0.00126404
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