A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6134n100



Internal ID20157750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106081902..106464172hg38UCSC Ensembl
chr6:106529777..106912047hg19UCSC Ensembl
chr6:106636470..107018740hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38382271
hg19382271
hg18382271
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1020047, nsv1025900
Samples
Known GenesATG5, PRDM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6134n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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