A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059762



Internal ID19148981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:20131902..20271953hg38UCSC Ensembl
Innerchr21:21504215..21644266hg19UCSC Ensembl
Innerchr21:20426086..20566137hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38140052
hg19140052
hg18140052
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599828
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059762
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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