A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3555396



Internal ID18853677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101684138..101738603hg38UCSC Ensembl
Innerchr15:102224341..102278806hg19UCSC Ensembl
Innerchr15:100041864..100096329hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3854466
hg1954466
hg1854466
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040277
Supporting Variants
Samples
Known GenesTARSL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3555396
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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