A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693939



Internal ID15430591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:20052675..20054653hg38UCSC Ensembl
Innerchr20:20033319..20035297hg19UCSC Ensembl
Innerchr20:19981319..19983297hg18UCSC Ensembl
Innerchr20:19981319..19983297hg17UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg381979
hg191979
hg181979
hg171979
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517467
Supporting Variants
Samples
Known GenesC20orf26, CRNKL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693939
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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