A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152406



Internal ID15877509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:40080107..40105280hg38UCSC Ensembl
Innerchr21:41452034..41477207hg19UCSC Ensembl
Innerchr21:40373904..40399077hg18UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3825174
hg1925174
hg1825174
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587488
Supporting Variants
SamplesHGDP01000
Known GenesDSCAM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152406
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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