A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796822



Internal ID18826024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46172086..46332633hg38UCSC Ensembl
Innerchr10:47543322..47703869hg19UCSC Ensembl
Innerchr10:47013328..47173875hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38160548
hg19160548
hg18160548
Variant TypeCNV loss
Copy Number1
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=41
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796822
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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