A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17593886



Internal ID21785929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98463744..98465922hg38UCSC Ensembl
chr9:101226026..101228204hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg382179
hg192179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6020006
Supporting Variants
Samples
Known GenesGABBR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17593886
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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