A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17585126



Internal ID21777169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135778892..135778892hg38UCSC Ensembl
chr9:138670738..138670738hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6088302
Supporting Variants
Samples
Known GenesKCNT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17585126
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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