A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785032



Internal ID19169283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:109043821..109066406hg38UCSC Ensembl
Innerchr2:109660277..109682862hg19UCSC Ensembl
Innerchr2:109026709..109049294hg18UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg3822586
hg1922586
hg1822586
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 HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785032
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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