A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005233



Internal ID18747764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..99044hg38UCSC Ensembl
Innerchr3:60333..140727hg19UCSC Ensembl
Innerchr3:35333..115727hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3880390
hg1980395
hg1880395
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4605n100
Supporting Variantsnssv3593529
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)nsv1005233
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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