A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17596912



Internal ID21788955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97690517..97690650hg38UCSC Ensembl
chr9:100452799..100452932hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012247
Supporting Variants
Samples
Known GenesXPA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17596912
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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