A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110656



Internal ID22019889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66342195..66344395hg38UCSC Ensembl
chr7:65807182..65809382hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg382201
hg192201
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576788
Samples
Known GenesTPST1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110656
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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