A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890847



Internal ID19185149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:54380472..54540195hg38UCSC Ensembl
Outerchr6:54380472..54540195hg38UCSC Ensembl
Innerchr6:54245270..54404993hg19UCSC Ensembl
Outerchr6:54245270..54404993hg19UCSC Ensembl
Innerchr6:54353229..54512952hg18UCSC Ensembl
Outerchr6:54353229..54512952hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38159724
hg19159724
hg18159724
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796897
Samples
Known GenesTINAG
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890847
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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