A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998366



Internal ID18811216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46760315..46804874hg38UCSC Ensembl
Innerchr3:46801805..46846364hg19UCSC Ensembl
Innerchr3:46776809..46821368hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3844560
hg1944560
hg1844560
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4736n100
Supporting Variantsnssv3591046, nssv3591049, nssv3591047, nssv3591048
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)nsv998366
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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