A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567140



Internal ID16354549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19991182..22111284hg38UCSC Ensembl
Innerchr15:20196435..22399235hg19UCSC Ensembl
Innerchr15:18456449..19900599hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382120103
hg192202801
hg181444151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4162n54
Supporting Variantsnssv836871
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N4, POTEB, POTEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567140
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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