A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239329



Internal ID20806369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58007392..58007945hg38UCSC Ensembl
chr16:58041296..58041849hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576355
Supporting Variants
Samples
Known GenesUSB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239329
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00026


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