A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264958



Internal ID20831998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25751913..25752658hg38UCSC Ensembl
chr4:25753535..25754280hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38746
hg19746
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567432
Supporting Variants
Samples
Known GenesSEL1L3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264958
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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