A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3649116



Internal ID18947397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:167185183..167305282hg38UCSC Ensembl
Innerchr5:166612188..166732287hg19UCSC Ensembl
Innerchr5:166544766..166664865hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38120100
hg19120100
hg18120100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032183
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)nssv3649116
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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