A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10892n54



Internal ID20144316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104813034..104814546hg38UCSC Ensembl
chr6:105260909..105262421hg19UCSC Ensembl
chr6:105367602..105369114hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg381513
hg191513
hg181513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604419, nsv604412, nsv604408, nsv604427, nsv604424
Samples
Known GenesHACE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10892n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss139
Observed Complex0
Frequencyn/a


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