A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435150



Internal ID22493020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:126804788..127311625hg38UCSC Ensembl
chr8:127817033..128323870hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38506838
hg19506838
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979072
Supporting Variants
Samples
Known GenesCCAT1, PCAT1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435150
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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