A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893413



Internal ID18837547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41410704..41454624hg38UCSC Ensembl
Outerchr21:41410704..41454624hg38UCSC Ensembl
Innerchr21:42782631..42826551hg19UCSC Ensembl
Outerchr21:42782631..42826551hg19UCSC Ensembl
Innerchr21:41704501..41748421hg18UCSC Ensembl
Outerchr21:41704501..41748421hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3843921
hg1943921
hg1843921
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790695
Samples
Known GenesMX1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893413
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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