A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5534889



Internal ID310633
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 StatusM
Merged Variants
Supporting Variantsnssv17697967
Samples
Known GenesESRRB
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5534889
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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