A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891759



Internal ID19186155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13257923..13264566hg38UCSC Ensembl
Outerchr10:13257923..13264566hg38UCSC Ensembl
Innerchr10:13299923..13306566hg19UCSC Ensembl
Outerchr10:13299923..13306566hg19UCSC Ensembl
Innerchr10:13339929..13346572hg18UCSC Ensembl
Outerchr10:13339929..13346572hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg386644
hg196644
hg186644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782337, essv25782259
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891759
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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