A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6555054



Internal ID9532457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:36032953..36034927hg38UCSC Ensembl
Outerchr21:36032796..36035080hg38UCSC Ensembl
Innerchr21:37405251..37407225hg19UCSC Ensembl
Outerchr21:37405094..37407378hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg382285
hg192285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665899
Supporting Variants
SamplesHG01080
Known GenesSETD4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6555054
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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