A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267028



Internal ID20834068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:71504079..71505142hg38UCSC Ensembl
chr5:70799906..70800969hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg381064
hg191064
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572656
Supporting Variants
Samples
Known GenesBDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267028
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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