A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3590987



Internal ID18542582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46760315..46790474hg38UCSC Ensembl
Innerchr3:46801805..46831964hg19UCSC Ensembl
Innerchr3:46776809..46806968hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3830160
hg1930160
hg1830160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006788
Supporting Variants
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)nssv3590987
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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