A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10935n54



Internal ID22778830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:130755882..130801153hg38UCSC Ensembl
chr6:131077027..131122295hg19UCSC Ensembl
chr6:131118720..131163988hg18UCSC Ensembl
Cytoband6q23.1
Allele length
AssemblyAllele length
hg3845272
hg1945269
hg1845269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604665, nsv604666
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10935n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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