A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890695



Internal ID22665723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177098012..177102221hg38UCSC Ensembl
chr5:176525013..176529222hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg384210
hg194210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420859
Samples
Known GenesFGFR4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890695
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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