A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002940



Internal ID19092157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:58775707..58858302hg38UCSC Ensembl
Innerchr3:58761434..58844028hg19UCSC Ensembl
Innerchr3:58736474..58819068hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3882596
hg1982595
hg1882595
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3731126
Samples
Known GenesC3orf67
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002940
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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