A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567312



Internal ID16354721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20242941..22303801hg38UCSC Ensembl
Innerchr15:20448194..22591752hg19UCSC Ensembl
Innerchr15:18708208..20093116hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382060861
hg192143559
hg181384909
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv837106, nssv837107
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567312
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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