A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268009



Internal ID20835049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146090022..146090272hg38UCSC Ensembl
chr5:145469585..145469835hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558378
Supporting Variants
Samples
Known GenesPLAC8L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268009
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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