A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012776



Internal ID18755308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6648983..6782709hg38UCSC Ensembl
Innerchr3:6690670..6824396hg19UCSC Ensembl
Innerchr3:6665670..6799396hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38133727
hg19133727
hg18133727
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4673n100
Supporting Variantsnssv3591825
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)nsv1012776
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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