A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002969



Internal ID19092186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:132266202..132282084hg38UCSC Ensembl
Innerchr3:131985046..132000928hg19UCSC Ensembl
Innerchr3:133467736..133483618hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3815883
hg1915883
hg1815883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4901n100
Supporting Variantsnssv3741468
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)nsv1002969
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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