A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780616



Internal ID18819757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:26527189..26537229hg38UCSC Ensembl
Innerchr22:26923155..26933195hg19UCSC Ensembl
Innerchr22:25253155..25263195hg18UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3810041
hg1910041
hg1810041
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893471
Supporting Variants
Samples
Known GenesTPST2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780616
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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