A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583516



Internal ID21775559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113411927..113412250hg38UCSC Ensembl
chr10:115171686..115172009hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6104923
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583516
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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