A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061476



Internal ID19150695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:19584599..19628605hg38UCSC Ensembl
Innerchr21:20956913..21000919hg19UCSC Ensembl
Innerchr21:19878784..19922790hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3844007
hg1944007
hg1844007
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599820
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)nsv1061476
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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