A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570732



Internal ID16011455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99789846..100224933hg38UCSC Ensembl
Innerchr15:100330051..100765138hg19UCSC Ensembl
Innerchr15:98147574..98582661hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38435088
hg19435088
hg18435088
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4769n54
Supporting Variantsnssv1148883
SamplesHGDP00684
Known GenesADAMTS17, DNM1P46
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570732
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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