A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17575317



Internal ID21767360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177554493..177554493hg38UCSC Ensembl
chr5:176981494..176981494hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6067084
Supporting Variants
Samples
Known GenesFAM193B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17575317
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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