A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586886



Internal ID20959957
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 StatusM
Merged Variants
Supporting Variantsnssv18242749
Samples
Known GenesLCMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586886
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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