A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151616



Internal ID15530999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:36003345..36087866hg38UCSC Ensembl
Innerchr21:37375643..37460164hg19UCSC Ensembl
Innerchr21:36297513..36382034hg18UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3884522
hg1984522
hg1884522
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587461
Supporting Variants
SamplesHGDP01029
Known GenesCBR1, LOC100133286, SETD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151616
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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