A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4162n54



Internal ID18996338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:19991182..22303801hg38UCSC Ensembl
chr15:20196435..22591752hg19UCSC Ensembl
chr15:18456449..20093116hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382312620
hg192395318
hg181636668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv567140, nsv567148, nsv567310, nsv567149, nsv567150, nsv567151, nsv567311
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)dgv4162n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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