A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv836885



Internal ID16130841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20009274..22303801hg38UCSC Ensembl
Innerchr15:20214527..22591752hg19UCSC Ensembl
Innerchr15:18474541..20093116hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382294528
hg192377226
hg181618576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv567151
Supporting Variants
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)nssv836885
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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