A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597519



Internal ID21789562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135774161..135774230hg38UCSC Ensembl
chr9:138666007..138666076hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6002617
Supporting Variants
Samples
Known GenesKCNT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597519
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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