A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17613097



Internal ID21805144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76757030..76757383hg38UCSC Ensembl
chr14:77223373..77223726hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6039804
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17613097
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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