A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242683



Internal ID20809723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23612758..23613632hg38UCSC Ensembl
chr16:23624079..23624953hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38875
hg19875
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589880
Supporting Variants
Samples
Known GenesPALB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242683
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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