A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003456



Internal ID19092674
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 StatusM
Merged Variants
Supporting Variantsnssv3591660
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)nsv1003456
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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