A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893562



Internal ID19184382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:228268852..228389624hg38UCSC Ensembl
Outerchr2:228268852..228389624hg38UCSC Ensembl
Innerchr2:229133568..229254340hg19UCSC Ensembl
Outerchr2:229133568..229254340hg19UCSC Ensembl
Innerchr2:228841812..228962584hg18UCSC Ensembl
Outerchr2:228841812..228962584hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38120773
hg19120773
hg18120773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800796, essv25781151
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893562
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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