A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3649118



Internal ID18947399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:167655795..167858003hg38UCSC Ensembl
Innerchr5:167082800..167285008hg19UCSC Ensembl
Innerchr5:167015378..167217586hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38202209
hg19202209
hg18202209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027805
Supporting Variants
Samples
Known GenesTENM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3649118
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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