A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780594



Internal ID19173882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57811677..58017021hg38UCSC Ensembl
Innerchr10:59571437..59776781hg19UCSC Ensembl
Innerchr10:59241443..59446787hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38205345
hg19205345
hg18205345
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891830
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=58
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780594
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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