A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893408



Internal ID19184228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:38036900..38072876hg38UCSC Ensembl
Outerchr21:38036900..38072876hg38UCSC Ensembl
Innerchr21:39409202..39444970hg19UCSC Ensembl
Outerchr21:39409202..39444970hg19UCSC Ensembl
Innerchr21:38331072..38366840hg18UCSC Ensembl
Outerchr21:38331072..38366840hg18UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3835977
hg1935769
hg1835769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778483
Samples
Known GenesDSCR4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893408
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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