A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5820175



Internal ID8797578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:36324065..36324747hg38UCSC Ensembl
Outerchr21:36324028..36324797hg38UCSC Ensembl
Innerchr21:37696363..37697045hg19UCSC Ensembl
Outerchr21:37696326..37697095hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38770
hg19770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2659831
Supporting Variants
SamplesHG00346
Known GenesMORC3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5820175
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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