A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268056



Internal ID20835096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162576658..162577202hg38UCSC Ensembl
chr5:162003664..162004208hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38545
hg19545
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560316
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268056
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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