A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890845



Internal ID19185147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:52765292..52804386hg38UCSC Ensembl
Outerchr6:52765292..52804386hg38UCSC Ensembl
Innerchr6:52630090..52669184hg19UCSC Ensembl
Outerchr6:52630090..52669184hg19UCSC Ensembl
Innerchr6:52738049..52777143hg18UCSC Ensembl
Outerchr6:52738049..52777143hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3839095
hg1939095
hg1839095
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788066
Samples
Known GenesGSTA1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890845
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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