A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3647975



Internal ID18599570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:119272480..119342573hg38UCSC Ensembl
Innerchr5:118608175..118678268hg19UCSC Ensembl
Innerchr5:118636074..118706167hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3870094
hg1970094
hg1870094
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024648
Supporting Variants
Samples
Known GenesTNFAIP8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3647975
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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