A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269728



Internal ID20836768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:89554881..89555615hg38UCSC Ensembl
chr5:88850698..88851432hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38735
hg19735
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568053
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269728
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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