A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269298



Internal ID20836338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149732022..149733517hg38UCSC Ensembl
chr6:150053158..150054653hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381496
hg191496
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558955
Supporting Variants
Samples
Known GenesNUP43
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269298
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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