A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049865



Internal ID21959098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44211732..44211798hg38UCSC Ensembl
chr21:45631615..45631681hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639439
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049865
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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