A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148884



Internal ID15878087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99817230..100057086hg38UCSC Ensembl
Innerchr15:100357435..100597291hg19UCSC Ensembl
Innerchr15:98174958..98414814hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38239857
hg19239857
hg18239857
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570733
Supporting Variants
SamplesHGDP01094
Known GenesADAMTS17
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148884
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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