A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239866



Internal ID20806906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12001379..12001753hg38UCSC Ensembl
chr16:12095236..12095610hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578482
Supporting Variants
Samples
Known GenesSNX29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239866
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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