A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781611



Internal ID18822180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46197060..46331115hg38UCSC Ensembl
Innerchr10:47568296..47702351hg19UCSC Ensembl
Innerchr10:47038302..47172357hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38134056
hg19134056
hg18134056
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 HumanHap 610
CommentsNumber of probes=50
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781611
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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