A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4827n54



Internal ID20138251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:760039..810673hg38UCSC Ensembl
chr16:810039..860673hg19UCSC Ensembl
chr16:750040..800674hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3850635
hg1950635
hg1850635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571024, nsv571026
SamplesHGDP00602
Known GenesCHTF18, GNG13, MIR662, MSLN, PRR25, RPUSD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4827n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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