A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697415



Internal ID15434067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:3858160..3870321hg38UCSC Ensembl
Innerchr20:3838807..3850968hg19UCSC Ensembl
Innerchr20:3786807..3798968hg18UCSC Ensembl
Innerchr20:3786807..3798968hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3812162
hg1912162
hg1812162
hg1712162
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520430
Supporting Variants
Samples
Known GenesMAVS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697415
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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