A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv946626



Internal ID15893896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33321856..33323918hg38UCSC Ensembl
Innerchr21:34694161..34696223hg19UCSC Ensembl
Innerchr21:33616031..33618093hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg382063
hg192063
hg182063
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587382
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)nssv946626
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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