A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269735



Internal ID20836775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8997889..9003223hg38UCSC Ensembl
chr5:8998001..9003335hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg385335
hg195335
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568708
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269735
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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