A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242824



Internal ID20809864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28168299..28168817hg38UCSC Ensembl
chr16:28179620..28180138hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587285
Supporting Variants
Samples
Known GenesXPO6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242824
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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