A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608084



Internal ID21800131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:89337221..89396245hg38UCSC Ensembl
chr13:89989475..90048499hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3859025
hg1959025
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028518
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608084
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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