A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620941



Internal ID21812988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45847589..45847680hg38UCSC Ensembl
chr20:44476228..44476319hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6044636
Supporting Variants
Samples
Known GenesACOT8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620941
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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