A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152379



Internal ID15854263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26104702..26265450hg38UCSC Ensembl
Innerchr20:26085338..26246086hg19UCSC Ensembl
Innerchr20:26033338..26194086hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38160749
hg19160749
hg18160749
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585771
Supporting Variants
Samples1780862057_A
Known GenesLOC284801, MIR663A, NCOR1P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152379
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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