A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785472



Internal ID19169221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:53597376..53766797hg38UCSC Ensembl
Innerchr10:55357136..55526557hg19UCSC Ensembl
Innerchr10:55027142..55196563hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38169422
hg19169422
hg18169422
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891811
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=78
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785472
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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