A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597929



Internal ID21789973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59489499..59489619hg38UCSC Ensembl
chr14:59956217..59956337hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031797
Supporting Variants
Samples
Known GenesJKAMP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597929
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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