A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239202



Internal ID20806242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20037233..20037923hg38UCSC Ensembl
chr16:20048555..20049245hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38691
hg19691
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581347
Supporting Variants
Samples
Known GenesGPR139
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239202
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00021


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