A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786985



Internal ID18823525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:25876144..25913383hg38UCSC Ensembl
Innerchr2:26099013..26136252hg19UCSC Ensembl
Innerchr2:25952517..25989756hg18UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3837240
hg1937240
hg1837240
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891648
Supporting Variants
Samples
Known GenesASXL2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786985
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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