A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891830



Internal ID19186226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57811677..58008290hg38UCSC Ensembl
Outerchr10:57811677..58017021hg38UCSC Ensembl
Innerchr10:59571437..59768050hg19UCSC Ensembl
Outerchr10:59571437..59776781hg19UCSC Ensembl
Innerchr10:59241443..59438056hg18UCSC Ensembl
Outerchr10:59241443..59446787hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38205345
hg19205345
hg18205345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780594, essv25785515, essv25780095
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891830
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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