A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624367



Internal ID21816414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5962341..5962670hg38UCSC Ensembl
chr20:5942987..5943316hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6048493
Supporting Variants
Samples
Known GenesMCM8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624367
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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