A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699791



Internal ID15436443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53574302..53604432hg38UCSC Ensembl
Innerchr19:54077556..54107686hg19UCSC Ensembl
Innerchr19:58769368..58799498hg18UCSC Ensembl
Innerchr19:58769368..58799498hg17UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3830131
hg1930131
hg1830131
hg1730131
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523944
Supporting Variants
Samples
Known GenesLOC284379, ZNF331
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699791
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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