A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012465



Internal ID19101682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:204470907..204484721hg38UCSC Ensembl
Innerchr2:205335630..205349444hg19UCSC Ensembl
Innerchr2:205043875..205057689hg18UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg3813815
hg1913815
hg1813815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3729331
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)nsv1012465
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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