A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3591963



Internal ID18890244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:11892508..11929836hg38UCSC Ensembl
Innerchr3:11933982..11971310hg19UCSC Ensembl
Innerchr3:11908982..11946310hg18UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3837329
hg1937329
hg1837329
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005190
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)nssv3591963
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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