A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18251513



Internal ID20818553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24751205..24751666hg38UCSC Ensembl
chr1:25077696..25078157hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535821
Supporting Variants
Samples
Known GenesCLIC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18251513
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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