A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890966



Internal ID19185362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152799769..152874502hg38UCSC Ensembl
Outerchr6:152799769..152874502hg38UCSC Ensembl
Innerchr6:153120904..153195637hg19UCSC Ensembl
Outerchr6:153120904..153195637hg19UCSC Ensembl
Innerchr6:153162597..153237330hg18UCSC Ensembl
Outerchr6:153162597..153237330hg18UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3874734
hg1974734
hg1874734
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788323
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890966
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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