A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920968



Internal ID22696191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135774444..135774507hg38UCSC Ensembl
chr9:138666290..138666353hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435074
Samples
Known GenesKCNT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920968
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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