A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6146n100



Internal ID20157762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131088144..131131160hg38UCSC Ensembl
chr6:131409284..131452300hg19UCSC Ensembl
chr6:131450977..131493993hg18UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3843017
hg1943017
hg1843017
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019112, nsv1016925
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6146n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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