A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059005



Internal ID20626045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:233627437..233628761hg38UCSC Ensembl
chr1:233763183..233764507hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg381325
hg191325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6315855
Supporting Variants
Samples
Known GenesKCNK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059005
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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