A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5911n100



Internal ID22791998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4255406..4473880hg38UCSC Ensembl
chr6:4255640..4474114hg19UCSC Ensembl
chr6:4200639..4419113hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38218475
hg19218475
hg18218475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1020205, nsv1027498, nsv1029501, nsv1026890
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)dgv5911n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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