A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272590



Internal ID20481808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26666988..26834710hg38UCSC Ensembl
chr6:26667216..26802489hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38167723
hg19135274
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753407
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272590
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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