A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890829



Internal ID19185131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32342087..32350952hg38UCSC Ensembl
Outerchr6:32342087..32350952hg38UCSC Ensembl
Innerchr6:32309864..32318729hg19UCSC Ensembl
Outerchr6:32309864..32318729hg19UCSC Ensembl
Innerchr6:32417842..32426707hg18UCSC Ensembl
Outerchr6:32417842..32426707hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg388866
hg198866
hg188866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782768
Samples
Known GenesC6orf10
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890829
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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