A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718224



Internal ID19016505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101491141..101612385hg38UCSC Ensembl
Innerchr15:102031344..102152588hg19UCSC Ensembl
Innerchr15:99848867..99970111hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38121245
hg19121245
hg18121245
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052172
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718224
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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