A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17562506



Internal ID21886861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154838616..154838616hg38UCSC Ensembl
chr5:154218176..154218176hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6080140
Supporting Variants
Samples
Known GenesFAXDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17562506
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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