A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6135641



Internal ID9661292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18624726..18628135hg38UCSC Ensembl
Outerchr21:18624689..18628185hg38UCSC Ensembl
Innerchr21:19997044..20000453hg19UCSC Ensembl
Outerchr21:19997007..20000503hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg383497
hg193497
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674181
Supporting Variants
SamplesNA19393
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6135641
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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