A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589733



Internal ID18888014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:43916653..43970460hg38UCSC Ensembl
Innerchr3:43958145..44011952hg19UCSC Ensembl
Innerchr3:43933149..43986956hg18UCSC Ensembl
Cytoband3p21.33
Allele length
AssemblyAllele length
hg3853808
hg1953808
hg1853808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000614
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)nssv3589733
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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