A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17593874



Internal ID21785917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96700487..96700643hg38UCSC Ensembl
chr9:99462769..99462925hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6011994
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17593874
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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