A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570731



Internal ID16358140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99789846..100059028hg38UCSC Ensembl
Innerchr15:100330051..100599233hg19UCSC Ensembl
Innerchr15:98147574..98416756hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38269183
hg19269183
hg18269183
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4770n54
Supporting Variantsnssv1148882
SamplesHGDP00986
Known GenesADAMTS17, DNM1P46
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570731
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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