A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267237



Internal ID20834277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:126552439..126553644hg38UCSC Ensembl
chr5:125888131..125889336hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg381206
hg191206
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558322
Supporting Variants
Samples
Known GenesALDH7A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267237
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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