A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17552630



Internal ID21876985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:357861..357861hg38UCSC Ensembl
chr5:357976..357976hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6077955
Supporting Variants
Samples
Known GenesAHRR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17552630
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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