A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801416



Internal ID19162466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:54685856..55411560hg38UCSC Ensembl
Innerchr10:56445616..57171320hg19UCSC Ensembl
Innerchr10:56115622..56841326hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38725705
hg19725705
hg18725705
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891814
Supporting Variants
Samples
Known GenesPCDH15, RNU6-59P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=183
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801416
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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