A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6088n100



Internal ID22792175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88997336..89048870hg38UCSC Ensembl
chr6:89707055..89758589hg19UCSC Ensembl
chr6:89763774..89815308hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3851535
hg1951535
hg1851535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015443, nsv1023619
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6088n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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