A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276156



Internal ID20843196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124490441..124490931hg38UCSC Ensembl
chr8:125502682..125503172hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569994
Supporting Variants
Samples
Known GenesTATDN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276156
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00042


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