A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694519



Internal ID15431171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:20880821..20883847hg38UCSC Ensembl
Innerchr20:20861464..20864490hg19UCSC Ensembl
Innerchr20:20809464..20812490hg18UCSC Ensembl
Innerchr20:20809464..20812490hg17UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg383027
hg193027
hg183027
hg173027
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521753
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694519
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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