A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679337



Internal ID15069303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42817913..43009507hg38UCSC Ensembl
Innerchr19:43322065..43513659hg19UCSC Ensembl
Innerchr19:48013905..48205499hg18UCSC Ensembl
Innerchr19:48013905..48205499hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38191595
hg19191595
hg18191595
hg17191595
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516973
Supporting Variants
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG6, PSG7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679337
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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