A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276137



Internal ID20843177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124174420..124174931hg38UCSC Ensembl
chr8:125186661..125187172hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556407
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276137
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00021


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