A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003495



Internal ID19092713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:161693262..161831189hg38UCSC Ensembl
Innerchr3:161411050..161548977hg19UCSC Ensembl
Innerchr3:162893744..163031671hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38137928
hg19137928
hg18137928
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4931n100
Supporting Variantsnssv3606410
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)nsv1003495
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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