A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787976



Internal ID18827053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46184058..46332633hg38UCSC Ensembl
Innerchr10:47555294..47703869hg19UCSC Ensembl
Innerchr10:47025300..47173875hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38148576
hg19148576
hg18148576
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=38
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787976
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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