A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12362n54



Internal ID22780257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139746713..139793689hg38UCSC Ensembl
chr8:140758956..140805932hg19UCSC Ensembl
chr8:140828138..140875114hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3846977
hg1946977
hg1846977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv612559, nsv612548
Samples1780862156_A, 1780862403_A
Known GenesTRAPPC9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12362n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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