A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266461



Internal ID20833501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:102657492..102658195hg38UCSC Ensembl
chr5:101993196..101993899hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38704
hg19704
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558466
Supporting Variants
Samples
Known GenesLINC00491
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266461
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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