A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108752



Internal ID22017986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:126690338..127316860hg38UCSC Ensembl
chr8:127702583..128329105hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38626523
hg19626523
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586664
Samples
Known GenesCCAT1, PCAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108752
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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