A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17596990



Internal ID21789033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88581757..88581757hg38UCSC Ensembl
chr9:91196672..91196672hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6095192
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17596990
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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