A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3732696



Internal ID19030977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:32042851..32098317hg38UCSC Ensembl
Innerchr21:33415164..33470630hg19UCSC Ensembl
Innerchr21:32337035..32392501hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3855467
hg1955467
hg1855467
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066591
Supporting Variants
Samples
Known GenesLINC00159
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3732696
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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