A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696666



Internal ID15433318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:35817343..35828354hg38UCSC Ensembl
Innerchr18:33397307..33408318hg19UCSC Ensembl
Innerchr18:31651305..31662316hg18UCSC Ensembl
Innerchr18:31651305..31662316hg17UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3811012
hg1911012
hg1811012
hg1711012
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519182
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696666
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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