A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569154



Internal ID16356563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34873165..34967175hg38UCSC Ensembl
Innerchr15:35165366..35259376hg19UCSC Ensembl
Innerchr15:32952658..33046668hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3894011
hg1994011
hg1894011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv840432
Samples
Known GenesAQR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569154
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