A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17591443



Internal ID21783486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135573267..135573323hg38UCSC Ensembl
chr9:138465113..138465169hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6000568
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17591443
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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