A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239867



Internal ID20806907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12007388..12008075hg38UCSC Ensembl
chr16:12101245..12101932hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38688
hg19688
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594916
Supporting Variants
Samples
Known GenesSNX29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239867
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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