A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3595202



Internal ID18546797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46767886..46806114hg38UCSC Ensembl
Innerchr3:46809376..46847604hg19UCSC Ensembl
Innerchr3:46784380..46822608hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3838229
hg1938229
hg1838229
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008120
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)nssv3595202
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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