A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5918n100



Internal ID20157534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10484627..10559867hg38UCSC Ensembl
chr6:10484860..10560100hg19UCSC Ensembl
chr6:10592846..10668086hg18UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3875241
hg1975241
hg1875241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1021023, nsv1034975, nsv1027649, nsv1023083
Samples
Known GenesGCNT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5918n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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