A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718229



Internal ID18669824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101618261..101712649hg38UCSC Ensembl
Innerchr15:102158464..102252852hg19UCSC Ensembl
Innerchr15:99975987..100070375hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3894389
hg1994389
hg1894389
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036401
Supporting Variants
Samples
Known GenesTARSL2, TM2D3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718229
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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