A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16891349



Internal ID168418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160070221..160070285hg38UCSC Ensembl
chr1:160040011..160040075hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433015
Supporting Variants
Samples
Known GenesKCNJ10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16891349
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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