A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266434



Internal ID20833474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55911362..55911652hg38UCSC Ensembl
chr4:56777528..56777818hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575555
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266434
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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