A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17623855



Internal ID21815902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21309595..21770096hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38460502
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106656
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17623855
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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