A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697989



Internal ID121655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76955608..76957279hg38UCSC Ensembl
chr14:77421951..77423622hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381672
hg191672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494447
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697989
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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