A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013922



Internal ID19103141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65202778..65224467hg38UCSC Ensembl
Innerchr3:65188453..65210142hg19UCSC Ensembl
Innerchr3:65163493..65185182hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3821690
hg1921690
hg1821690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4761n100
Supporting Variantsnssv3731179
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)nsv1013922
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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