A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052238



Internal ID21961471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43635449..43635539hg38UCSC Ensembl
chr20:42264089..42264179hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634726
Samples
Known GenesIFT52
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052238
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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