A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569808



Internal ID16010531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:69035886..69100053hg38UCSC Ensembl
Innerchr15:69328226..69392393hg19UCSC Ensembl
Innerchr15:67115280..67179447hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3864168
hg1964168
hg1864168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv844367
Samples
Known GenesLINC00277, MIR548H4, NOX5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569808
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