A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746596



Internal ID19044877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:117005259..117092173hg38UCSC Ensembl
Innerchr5:116340955..116427869hg19UCSC Ensembl
Innerchr5:116368854..116455768hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3886915
hg1986915
hg1886915
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028067
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)nssv3746596
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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