A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17695985



Internal ID119651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60896651..60930145hg38UCSC Ensembl
chr14:61363369..61396863hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3833495
hg1933495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513298
Supporting Variants
Samples
Known GenesMNAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17695985
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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