A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3600153



Internal ID18898434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:35871831..35949068hg38UCSC Ensembl
Innerchr21:37244129..37321366hg19UCSC Ensembl
Innerchr21:36165999..36243236hg18UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3877238
hg1977238
hg1877238
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056646
Supporting Variants
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)nssv3600153
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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