A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241293



Internal ID20808333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71684175..71685098hg38UCSC Ensembl
chr16:71718078..71719001hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg38924
hg19924
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581133
Supporting Variants
Samples
Known GenesPHLPP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241293
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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