A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267751



Internal ID20834791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96325210..96325450hg38UCSC Ensembl
chr5:95660914..95661154hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561112
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267751
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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