A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275524



Internal ID20842564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123233303..123233411hg38UCSC Ensembl
chr8:124245543..124245651hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559018
Supporting Variants
Samples
Known GenesC8orf76, ZHX1-C8ORF76
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275524
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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