A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267048



Internal ID20834088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:72311863..72312694hg38UCSC Ensembl
chr5:71607690..71608521hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38832
hg19832
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566772
Supporting Variants
Samples
Known GenesMRPS27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267048
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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