A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040723



Internal ID21950062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11875738..11875817hg38UCSC Ensembl
chr21:9755342..9755421hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639104
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040723
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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