A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005353



Internal ID18747884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:181888080..182015301hg38UCSC Ensembl
Innerchr3:181605868..181733089hg19UCSC Ensembl
Innerchr3:183088562..183215783hg18UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38127222
hg19127222
hg18127222
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3738454
Samples
Known GenesLOC100996490
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005353
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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