A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10840n54



Internal ID22778735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:92390188..92430198hg38UCSC Ensembl
chr6:93099906..93139916hg19UCSC Ensembl
chr6:93156627..93196637hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3840011
hg1940011
hg1840011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604147, nsv604146
Samples1780854495_A, HGDP00948
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10840n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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