A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12252n54



Internal ID22780147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105784312..105785047hg38UCSC Ensembl
chr8:106796540..106797275hg19UCSC Ensembl
chr8:106865716..106866451hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38736
hg19736
hg18736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv611838, nsv611839
Samples
Known GenesZFPM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12252n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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