A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698236



Internal ID15088202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:31356870..31357229hg38UCSC Ensembl
Innerchr18:28936833..28937192hg19UCSC Ensembl
Innerchr18:27190831..27191190hg18UCSC Ensembl
Innerchr18:27190831..27191190hg17UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38360
hg19360
hg18360
hg17360
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521618
Supporting Variants
Samples
Known GenesDSG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698236
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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