A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569966



Internal ID16357375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73368223..73368898hg38UCSC Ensembl
Innerchr15:73660564..73661239hg19UCSC Ensembl
Innerchr15:71447617..71448292hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38676
hg19676
hg18676
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv845254, nssv845253
Samples
Known GenesHCN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569966
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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