A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060321



Internal ID21969554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17380673..17382764hg38UCSC Ensembl
chr21:18752992..18755083hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg382092
hg192092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638360
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060321
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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