A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249378



Internal ID20816418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:224403113..224403655hg38UCSC Ensembl
chr1:224590815..224591357hg19UCSC Ensembl
Cytoband1q42.11
Allele length
AssemblyAllele length
hg38543
hg19543
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552060
Supporting Variants
Samples
Known GenesWDR26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249378
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00029


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