A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800672



Internal ID19165857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1689422..1750935hg38UCSC Ensembl
Innerchr1:1620861..1682374hg19UCSC Ensembl
Innerchr1:1610720..1672234hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3861514
hg1961514
hg1861515
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891747
Supporting Variants
Samples
Known GenesCDK11A, CDK11B, MMP23A, SLC35E2, SLC35E2B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800672
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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