A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267351



Internal ID20834391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:134776117..134778865hg38UCSC Ensembl
chr5:134111807..134114555hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg382749
hg192749
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559973
Supporting Variants
Samples
Known GenesDDX46
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267351
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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