A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5281n100



Internal ID20156897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68554293..68607148hg38UCSC Ensembl
chr4:69420011..69472866hg19UCSC Ensembl
chr4:69102606..69155461hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3852856
hg1952856
hg1852856
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1007311, nsv1006279, nsv1007680
Samples
Known GenesUGT2B17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5281n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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