A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3533560



Internal ID18485155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102605524..102784666hg38UCSC Ensembl
Innerchr14:103071861..103251003hg19UCSC Ensembl
Innerchr14:102141614..102320756hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38179143
hg19179143
hg18179143
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044276
Supporting Variants
Samples
Known GenesRCOR1, TRAF3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3533560
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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