A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17555761



Internal ID21880116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14689431..14689431hg38UCSC Ensembl
chr5:14689540..14689540hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6080266
Supporting Variants
Samples
Known GenesFAM105B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17555761
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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