A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691264



Internal ID15427916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26327161..26328619hg38UCSC Ensembl
Innerchr20:26307797..26309255hg19UCSC Ensembl
Innerchr20:26255797..26257255hg18UCSC Ensembl
Innerchr20:26255797..26257255hg17UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg381459
hg191459
hg181459
hg171459
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519490
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691264
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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