A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18270346



Internal ID20837386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:99354756..100525677hg38UCSC Ensembl
chr5:98690460..99861381hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg381170922
hg191170922
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569018
Supporting Variants
Samples
Known GenesLOC100133050
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18270346
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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