A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17559371



Internal ID21883726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147183647..147183647hg38UCSC Ensembl
chr5:146563210..146563210hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6061033
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17559371
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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