A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268369



Internal ID20835409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42524136..42705513hg38UCSC Ensembl
chr5:42524238..42705615hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38181378
hg19181378
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566946
Supporting Variants
Samples
Known GenesGHR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268369
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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