A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456867



Internal ID234925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177098016..177102222hg38UCSC Ensembl
chr5:176525017..176529223hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg384207
hg194207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16978222
Samples
Known GenesFGFR4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456867
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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