A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267389



Internal ID20834429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:136972983..136973552hg38UCSC Ensembl
chr5:136308672..136309241hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38570
hg19570
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566900
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267389
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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