A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569994



Internal ID16010717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:75044388..75155432hg38UCSC Ensembl
Innerchr15:75336729..75447773hg19UCSC Ensembl
Innerchr15:73123782..73234826hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38111045
hg19111045
hg18111045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv845288
Samples
Known GenesPPCDC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569994
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