A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046622



Internal ID21955859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36022462..36030052hg38UCSC Ensembl
chr20:34610384..34617974hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg387591
hg197591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628381
Samples
Known GenesCNBD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046622
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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