A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17549991



Internal ID21874346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:83060042..83060042hg38UCSC Ensembl
chr5:82355861..82355861hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg382563
hg192563
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6067934
Supporting Variants
Samples
Known GenesTMEM167A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17549991
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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