A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3591641



Internal ID18889922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:5327116..5648141hg38UCSC Ensembl
Innerchr3:5368801..5689828hg19UCSC Ensembl
Innerchr3:5343801..5664828hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38321026
hg19321028
hg18321028
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009089
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)nssv3591641
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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