A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543733



Internal ID21868088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120818947..120819174hg38UCSC Ensembl
chr3:120537794..120538021hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107513
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543733
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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