A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17557489



Internal ID21881844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187413745..187424394hg38UCSC Ensembl
chr3:187131533..187142182hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3810650
hg1910650
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103794
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17557489
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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