A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570259



Internal ID16357668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:83783300..83788593hg38UCSC Ensembl
Innerchr15:84452052..84457345hg19UCSC Ensembl
Innerchr15:82243056..82248349hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg385294
hg195294
hg185294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv847572
Samples
Known GenesADAMTSL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570259
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer