A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17577823



Internal ID21769866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96648933..96648985hg38UCSC Ensembl
chr9:99411215..99411267hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014561
Supporting Variants
Samples
Known GenesAAED1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17577823
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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