A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12025n54



Internal ID20145449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:16127153..16171585hg38UCSC Ensembl
chr8:15984662..16029094hg19UCSC Ensembl
chr8:16029033..16073465hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3844433
hg1944433
hg1844433
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610598, nsv610597
SamplesHGDP01172
Known GenesMSR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12025n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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