A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000762



Internal ID18743293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41862178..42019253hg38UCSC Ensembl
Innerchr3:41903670..42060745hg19UCSC Ensembl
Innerchr3:41878674..42035749hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38157076
hg19157076
hg18157076
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4726n100
Supporting Variantsnssv3589715
Samples
Known GenesULK4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1000762
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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