A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3642053



Internal ID18940334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:50159790..50225746hg38UCSC Ensembl
Innerchr5:49455624..49521580hg19UCSC Ensembl
Innerchr5:49491381..49557337hg18UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg3865957
hg1965957
hg1865957
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032680
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)nssv3642053
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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