A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17592299



Internal ID21784342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79507026..79507227hg38UCSC Ensembl
chr10:81266782..81266983hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019029
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17592299
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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