A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17577105



Internal ID21769148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:163418429..163429490hg38UCSC Ensembl
chr5:162845435..162856496hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3811062
hg1911062
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103623
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17577105
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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