A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268762



Internal ID20835802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154822206..154823019hg38UCSC Ensembl
chr5:154201766..154202579hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38814
hg19814
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569942
Supporting Variants
Samples
Known GenesFAXDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268762
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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