A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152378



Internal ID15876998
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
SamplesHGDP00924
Known GenesLOC284801, MIR663A, NCOR1P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152378
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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