A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10944n54



Internal ID19003120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134269029..134271001hg38UCSC Ensembl
chr6:134590167..134592139hg19UCSC Ensembl
chr6:134631860..134633832hg18UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg381973
hg191973
hg181973
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604705, nsv604706
Samples
Known GenesSGK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10944n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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