A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616719



Internal ID21808766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76347430..76347865hg38UCSC Ensembl
chr14:76813773..76814208hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036181
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616719
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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