A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268639



Internal ID20835679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147252428..147258245hg38UCSC Ensembl
chr5:146631991..146637808hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg385818
hg195818
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559436
Supporting Variants
Samples
Known GenesSTK32A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268639
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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