A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057149



Internal ID21966382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43701682..43717727hg38UCSC Ensembl
chr21:45121563..45137608hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3816046
hg1916046
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643919
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057149
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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