A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568118



Internal ID20941189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:167593055..167820142hg38UCSC Ensembl
chr4:168514206..168741293hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38227088
hg19227088
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264338
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568118
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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