A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570775



Internal ID16011498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99963234..100019563hg38UCSC Ensembl
Innerchr15:100503439..100559768hg19UCSC Ensembl
Innerchr15:98320962..98377291hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3856330
hg1956330
hg1856330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv850861
Samples
Known GenesADAMTS17
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570775
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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