A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267881



Internal ID20834921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:130476904..130477361hg38UCSC Ensembl
chr5:129812597..129813054hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg38458
hg19458
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574901
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267881
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00018


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