A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891811



Internal ID19186207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:53597376..53766797hg38UCSC Ensembl
Outerchr10:53597376..53766797hg38UCSC Ensembl
Innerchr10:55357136..55526557hg19UCSC Ensembl
Outerchr10:55357136..55526557hg19UCSC Ensembl
Innerchr10:55027142..55196563hg18UCSC Ensembl
Outerchr10:55027142..55196563hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38169422
hg19169422
hg18169422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785472
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891811
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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