A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264192



Internal ID20831232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119067740..119073925hg38UCSC Ensembl
chr4:119988895..119995080hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg386186
hg196186
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574684
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264192
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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