A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv567169



Internal ID16354578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20029080..21065301hg38UCSC Ensembl
Innerchr15:20234333..21270630hg19UCSC Ensembl
Innerchr15:18494347..19535289hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381036222
hg191036298
hg181040943
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4166n54
Supporting Variantsnssv836907, nssv836906
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv567169
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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