A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266530



Internal ID20833570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:65741459..66045782hg38UCSC Ensembl
chr4:66607177..66911500hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38304324
hg19304324
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570812
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266530
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00013


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