A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250043



Internal ID20817083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23827455..23828530hg38UCSC Ensembl
chr1:24153945..24155020hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381076
hg191076
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548580
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250043
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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