A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003910



Internal ID18746441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18655..104040hg38UCSC Ensembl
Innerchr3:60333..145723hg19UCSC Ensembl
Innerchr3:35333..120723hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3885386
hg1985391
hg1885391
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4605n100
Supporting Variantsnssv3590187, nssv3590188
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)nsv1003910
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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