A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567199



Internal ID16354608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20054126..20762254hg38UCSC Ensembl
Innerchr15:20259379..20967583hg19UCSC Ensembl
Innerchr15:18519393..19227614hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38708129
hg19708205
hg18708222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4174n54
Supporting Variantsnssv836948
Samples
Known GenesCHEK2P2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567199
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