A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893411



Internal ID19184231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:39904871..39919498hg38UCSC Ensembl
Outerchr21:39904871..39919498hg38UCSC Ensembl
Innerchr21:41276796..41291423hg19UCSC Ensembl
Outerchr21:41276796..41291423hg19UCSC Ensembl
Innerchr21:40198666..40213293hg18UCSC Ensembl
Outerchr21:40198666..40213293hg18UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3814628
hg1914628
hg1814628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799575, essv25798421
Samples
Known GenesPCP4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893411
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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