A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148885



Internal ID15528781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99817230..100224933hg38UCSC Ensembl
Innerchr15:100357435..100765138hg19UCSC Ensembl
Innerchr15:98174958..98582661hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38407704
hg19407704
hg18407704
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570734
Supporting Variants
SamplesHGDP00686
Known GenesADAMTS17
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148885
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer