A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788828



Internal ID18830989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46166132..46331115hg38UCSC Ensembl
Innerchr10:47537368..47702351hg19UCSC Ensembl
Innerchr10:47007374..47172357hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38164984
hg19164984
hg18164984
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=54
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788828
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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