A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567367



Internal ID16354776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20370594..20689298hg38UCSC Ensembl
Innerchr15:20575847..20894627hg19UCSC Ensembl
Innerchr15:18835861..19194596hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38318705
hg19318781
hg18358736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4194n54
Supporting Variantsnssv837167
Samples
Known GenesGOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567367
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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