A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565796



Internal ID20938867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158363994..158435528hg38UCSC Ensembl
chr4:159285146..159356680hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3871535
hg1971535
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264216
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565796
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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