A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106656



Internal ID22015890
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 StatusM
Merged Variants
Supporting Variantsnssv17623855
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106656
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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