A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151355



Internal ID15876581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37381254..37441251hg38UCSC Ensembl
Innerchr20:36009657..36069653hg19UCSC Ensembl
Innerchr20:35443071..35503067hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3859998
hg1959997
hg1859997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585961
Supporting Variants
SamplesHGDP00864
Known GenesSRC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151355
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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