A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665016



Internal ID15054982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54036316..54036948hg38UCSC Ensembl
Innerchr20:52652855..52653487hg19UCSC Ensembl
Innerchr20:52086262..52086894hg18UCSC Ensembl
Innerchr20:52086262..52086894hg17UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38633
hg19633
hg18633
hg17633
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517164
Supporting Variants
Samples
Known GenesBCAS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665016
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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