A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066285



Internal ID18808816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:31814829..31932375hg38UCSC Ensembl
Innerchr21:33187141..33304687hg19UCSC Ensembl
Innerchr21:32109012..32226558hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38117547
hg19117547
hg18117547
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600120
Samples
Known GenesHUNK
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066285
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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