A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269622



Internal ID20836662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:82189623..82190552hg38UCSC Ensembl
chr5:81485442..81486371hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg38930
hg19930
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572519
Supporting Variants
Samples
Known GenesATG10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269622
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00024


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