A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570385



Internal ID16011108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:88806095..88830608hg38UCSC Ensembl
Innerchr15:89349326..89373839hg19UCSC Ensembl
Innerchr15:87150330..87174843hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3824514
hg1924514
hg1824514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv848199
Samples
Known GenesACAN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570385
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