A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263659



Internal ID20830699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:122725777..122727309hg38UCSC Ensembl
chr4:123646932..123648464hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg381533
hg191533
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575165
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263659
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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