A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242749



Internal ID20809789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25161357..25162432hg38UCSC Ensembl
chr16:25172678..25173753hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381076
hg191076
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586886
Supporting Variants
Samples
Known GenesLCMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242749
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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