A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10890n54



Internal ID20144314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104813034..104813943hg38UCSC Ensembl
chr6:105260909..105261818hg19UCSC Ensembl
chr6:105367602..105368511hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38910
hg19910
hg18910
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604405, nsv604414, nsv604409
Samples
Known GenesHACE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10890n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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