A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3642132



Internal ID18940413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:53809039..53883127hg38UCSC Ensembl
Innerchr5:53104869..53178957hg19UCSC Ensembl
Innerchr5:53140626..53214714hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3874089
hg1974089
hg1874089
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019194
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)nssv3642132
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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