A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697960



Internal ID121626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76421597..76434642hg38UCSC Ensembl
chr14:76887940..76900985hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3813046
hg1913046
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500651
Supporting Variants
Samples
Known GenesESRRB
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697960
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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