A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047790



Internal ID21957023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33805712..33805782hg38UCSC Ensembl
chr21:35178016..35178086hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646538
Samples
Known GenesITSN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047790
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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