A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570778



Internal ID16358187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99974771..99976763hg38UCSC Ensembl
Innerchr15:100514976..100516968hg19UCSC Ensembl
Innerchr15:98332499..98334491hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381993
hg191993
hg181993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv850864
Samples
Known GenesADAMTS17
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570778
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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