A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746601



Internal ID19044882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:120394106..120446067hg38UCSC Ensembl
Innerchr5:119729801..119781762hg19UCSC Ensembl
Innerchr5:119757700..119809661hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3851962
hg1951962
hg1851962
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020655
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)nssv3746601
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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