A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890957



Internal ID19185353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:141995040..142055314hg38UCSC Ensembl
Outerchr6:141995040..142055314hg38UCSC Ensembl
Innerchr6:142316177..142376451hg19UCSC Ensembl
Outerchr6:142316177..142376451hg19UCSC Ensembl
Innerchr6:142357870..142418144hg18UCSC Ensembl
Outerchr6:142357870..142418144hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3860275
hg1960275
hg1860275
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786922
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890957
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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