A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013833



Internal ID19103052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:84332981..84507805hg38UCSC Ensembl
Innerchr3:84382132..84556956hg19UCSC Ensembl
Innerchr3:84464822..84639646hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38174825
hg19174825
hg18174825
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596254
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)nsv1013833
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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