A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3640469



Internal ID18938750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:98149425..98227408hg38UCSC Ensembl
Innerchr5:97485129..97563112hg19UCSC Ensembl
Innerchr5:97510885..97588868hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3877984
hg1977984
hg1877984
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029815
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)nssv3640469
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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