A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010198



Internal ID18752729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3934721..4211337hg38UCSC Ensembl
Innerchr3:3976405..4253021hg19UCSC Ensembl
Innerchr3:3951405..4228021hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38276617
hg19276617
hg18276617
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4641n100
Supporting Variantsnssv3590399
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)nsv1010198
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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