A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267095



Internal ID20834135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:91067443..91068345hg38UCSC Ensembl
chr5:90363260..90364162hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38903
hg19903
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556109
Supporting Variants
Samples
Known GenesGPR98
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267095
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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