A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266386



Internal ID20833426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52211429..52213377hg38UCSC Ensembl
chr4:53077595..53079543hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381949
hg191949
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570657
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266386
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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