A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3555376



Internal ID18506971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101587705..101790849hg38UCSC Ensembl
Innerchr15:102127908..102331052hg19UCSC Ensembl
Innerchr15:99945431..100148575hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38203145
hg19203145
hg18203145
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051784
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)nssv3555376
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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