A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697521



Internal ID15434173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:29628544..29754818hg38UCSC Ensembl
Innerchr18:27208509..27334783hg19UCSC Ensembl
Innerchr18:25462507..25588781hg18UCSC Ensembl
Innerchr18:25462507..25588781hg17UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38126275
hg19126275
hg18126275
hg17126275
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520618
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697521
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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