A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694905



Internal ID15431557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:66928790..66965230hg38UCSC Ensembl
Innerchr18:64596027..64632467hg19UCSC Ensembl
Innerchr18:62747007..62783447hg18UCSC Ensembl
Innerchr18:62747007..62783447hg17UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3836441
hg1936441
hg1836441
hg1736441
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522131
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694905
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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