A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787766



Internal ID18815494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46330334hg38UCSC Ensembl
Innerchr10:47543322..47701570hg19UCSC Ensembl
Innerchr10:47013328..47171576hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38158249
hg19158249
hg18158249
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891801
Supporting Variants
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=39
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787766
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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