A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697966



Internal ID121632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76485216..76485427hg38UCSC Ensembl
chr14:76951559..76951770hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5498036
Supporting Variants
Samples
Known GenesESRRB
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697966
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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