A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16897906



Internal ID172761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:233667393..233667447hg38UCSC Ensembl
chr1:233803139..233803193hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5450335
Supporting Variants
Samples
Known GenesKCNK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16897906
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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