A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241439



Internal ID20808479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74980427..74980898hg38UCSC Ensembl
chr16:75014325..75014796hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38472
hg19472
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587791
Supporting Variants
Samples
Known GenesWDR59
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241439
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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