A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893407



Internal ID19184227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33766022..33792445hg38UCSC Ensembl
Outerchr21:33766022..33792445hg38UCSC Ensembl
Innerchr21:35138326..35164749hg19UCSC Ensembl
Outerchr21:35138326..35164749hg19UCSC Ensembl
Innerchr21:34060196..34086619hg18UCSC Ensembl
Outerchr21:34060196..34086619hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3826424
hg1926424
hg1826424
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784588
Samples
Known GenesITSN1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893407
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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