A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569600



Internal ID20942671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:134171656..134177442hg38UCSC Ensembl
chr4:135092811..135098597hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg385787
hg195787
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263103
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569600
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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