A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17595788



Internal ID21787831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96400741..96400741hg38UCSC Ensembl
chr9:99163023..99163023hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6082919
Supporting Variants
Samples
Known GenesZNF367
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17595788
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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