A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570260



Internal ID16357669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:83871411..83875030hg38UCSC Ensembl
Innerchr15:84540163..84543782hg19UCSC Ensembl
Innerchr15:82331167..82334786hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg383620
hg193620
hg183620
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv847573, nssv847574, nssv847575
Samples
Known GenesADAMTSL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570260
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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