A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10889n54



Internal ID20144313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104797546..104814546hg38UCSC Ensembl
chr6:105245421..105262421hg19UCSC Ensembl
chr6:105352114..105369114hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3817001
hg1917001
hg1817001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604403, nsv604404
Samples
Known GenesHACE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10889n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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