A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788489



Internal ID18831225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46184058..46332377hg38UCSC Ensembl
Innerchr10:47555294..47703613hg19UCSC Ensembl
Innerchr10:47025300..47173619hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38148320
hg19148320
hg18148320
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 HumanHap 610
CommentsNumber of probes=52
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788489
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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