A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3591660



Internal ID18889941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:5517792..5934762hg38UCSC Ensembl
Innerchr3:5559479..5976449hg19UCSC Ensembl
Innerchr3:5534479..5951449hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38416971
hg19416971
hg18416971
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003456
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)nssv3591660
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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