A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600364



Internal ID21792411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90175890..90176850hg38UCSC Ensembl
chr14:90642234..90643194hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38961
hg19961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036160
Supporting Variants
Samples
Known GenesKCNK13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600364
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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