A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893537



Internal ID19184357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:205870581..205974714hg38UCSC Ensembl
Outerchr2:205870581..205974714hg38UCSC Ensembl
Innerchr2:206735305..206839438hg19UCSC Ensembl
Outerchr2:206735305..206839438hg19UCSC Ensembl
Innerchr2:206443550..206547683hg18UCSC Ensembl
Outerchr2:206443550..206547683hg18UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38104134
hg19104134
hg18104134
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799825
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893537
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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