A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267441



Internal ID20834481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160178451..160179996hg38UCSC Ensembl
chr5:159605458..159607003hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg381546
hg191546
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563014
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267441
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00018


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