A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583922



Internal ID21775965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91235384..91245482hg38UCSC Ensembl
chr9:93997666..94007764hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3810099
hg1910099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6013494
Supporting Variants
Samples
Known GenesAUH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583922
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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