A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv946162



Internal ID16240118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:19170535..20271880hg38UCSC Ensembl
Innerchr21:20542853..21644193hg19UCSC Ensembl
Innerchr21:19464724..20566064hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg381101346
hg191101341
hg181101341
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587161
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv946162
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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