A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv391n21



Internal ID22766583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106227944..106255743hg38UCSC Ensembl
chr6:106675819..106703618hg19UCSC Ensembl
chr6:106782512..106810311hg18UCSC Ensembl
chr6:106782512..106810311hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3827800
hg1927800
hg1827800
hg1727800
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv520329, nsv521859
Samples
Known GenesATG5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv391n21
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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