A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv836952



Internal ID16130908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20054126..21065301hg38UCSC Ensembl
Innerchr15:20259379..21270630hg19UCSC Ensembl
Innerchr15:18519393..19535289hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381011176
hg191011252
hg181015897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv567203
Supporting Variants
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)nssv836952
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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