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nsv5436095

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:96

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 84 SVs from 15 studies. See in: genome view    
Submitted genomic231,118,287-231,118,382Question Mark
Overlapping variant regions from other studies: 84 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):231,983,001-231,983,096Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5436095Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2231,118,287231,118,382
nsv5436095RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2231,983,001231,983,096

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16928553duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16928553Submitted genomicNC_000002.12:g.231
118287_231118382du
p
GRCh38 (hg38)NC_000002.12Chr2231,118,287231,118,382
nssv16928553RemappedPerfectNC_000002.11:g.231
983001_231983096du
p
GRCh37.p13First PassNC_000002.11Chr2231,983,001231,983,096

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)
nssv16928553<0.00116404
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