A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891822



Internal ID19186218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:56323877..56361440hg38UCSC Ensembl
Outerchr10:56323877..56361440hg38UCSC Ensembl
Innerchr10:58083638..58121201hg19UCSC Ensembl
Outerchr10:58083638..58121201hg19UCSC Ensembl
Innerchr10:57753644..57791207hg18UCSC Ensembl
Outerchr10:57753644..57791207hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3837564
hg1937564
hg1837564
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797242
Samples
Known GenesZWINT
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891822
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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