A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17604822



Internal ID21796869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51741194..51742017hg38UCSC Ensembl
chr14:52207912..52208735hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38824
hg19824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023839
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17604822
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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