A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697967



Internal ID121633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76496351..76496401hg38UCSC Ensembl
chr14:76962694..76962744hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534889
Supporting Variants
Samples
Known GenesESRRB
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697967
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.156789


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