A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266532



Internal ID20833572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:65748733..65771634hg38UCSC Ensembl
chr4:66614451..66637352hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3822902
hg1922902
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555892
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266532
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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