A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3642108



Internal ID18940389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:50159790..50273114hg38UCSC Ensembl
Innerchr5:49455624..49568948hg19UCSC Ensembl
Innerchr5:49491381..49604705hg18UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg38113325
hg19113325
hg18113325
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034447
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)nssv3642108
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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