A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17550509



Internal ID21874864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69220605..69220605hg38UCSC Ensembl
chr5:68516432..68516432hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6065925
Supporting Variants
Samples
Known GenesMRPS36
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17550509
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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