A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797850



Internal ID19167736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:109034560..109070112hg38UCSC Ensembl
Innerchr2:109651016..109686568hg19UCSC Ensembl
Innerchr2:109017448..109053000hg18UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg3835553
hg1935553
hg1835553
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893026
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797850
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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