A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17634905



Internal ID21826952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37572180..37572418hg38UCSC Ensembl
chr20:36200582..36200820hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6047076
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17634905
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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