A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7268n100



Internal ID20158884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91106767..91173829hg38UCSC Ensembl
chr8:92118995..92186057hg19UCSC Ensembl
chr8:92188171..92255233hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3867063
hg1967063
hg1867063
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024251, nsv1027865, nsv1028288
Samples
Known GenesLRRC69
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7268n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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