A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056646



Internal ID19145865
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 StatusM
Merged Variants
Supporting Variantsnssv3600153
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)nsv1056646
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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