A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv373n21



Internal ID20132094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10469593..10542543hg38UCSC Ensembl
chr6:10469826..10542776hg19UCSC Ensembl
chr6:10577812..10650762hg18UCSC Ensembl
chr6:10577812..10650762hg17UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3872951
hg1972951
hg1872951
hg1772951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv522231, nsv520598
Samples
Known GenesGCNT2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv373n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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