A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10830n54



Internal ID22778725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85879572..85965782hg38UCSC Ensembl
chr6:86589290..86675500hg19UCSC Ensembl
chr6:86646009..86732219hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3886211
hg1986211
hg1886211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604098, nsv604097
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10830n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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