A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263716



Internal ID20830756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:127770455..127771029hg38UCSC Ensembl
chr4:128691610..128692184hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38575
hg19575
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566365
Supporting Variants
Samples
Known GenesSLC25A31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263716
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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