A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269132



Internal ID20836172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61457533..61458883hg38UCSC Ensembl
chr5:60753360..60754710hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg381351
hg191351
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562162
Supporting Variants
Samples
Known GenesZSWIM6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269132
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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