A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17623335



Internal ID21815382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25503309..25503417hg38UCSC Ensembl
chr20:25483945..25484053hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6058073
Supporting Variants
Samples
Known GenesNINL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17623335
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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