A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17561000



Internal ID21885355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176368724..176368724hg38UCSC Ensembl
chr5:175795727..175795727hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6070832
Supporting Variants
Samples
Known GenesARL10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17561000
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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