A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17529570



Internal ID21853927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:211111806..211111924hg38UCSC Ensembl
chr1:211285148..211285266hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982538
Supporting Variants
Samples
Known GenesKCNH1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17529570
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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