A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269729



Internal ID20836769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:89555242..89555397hg38UCSC Ensembl
chr5:88851059..88851214hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559086
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269729
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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