A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5998n100



Internal ID22792085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:64996668..65190495hg38UCSC Ensembl
chr6:65706561..65900388hg19UCSC Ensembl
chr6:65763282..65957109hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38193828
hg19193828
hg18193828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018528, nsv1018829
Samples
Known GenesEYS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5998n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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