A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3642091



Internal ID18940372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:50159790..50260292hg38UCSC Ensembl
Innerchr5:49455624..49556126hg19UCSC Ensembl
Innerchr5:49491381..49591883hg18UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg38100503
hg19100503
hg18100503
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017682
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)nssv3642091
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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