A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572860



Internal ID20945931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102602532..102603363hg38UCSC Ensembl
chr4:103523689..103524520hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38832
hg19832
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263389
Samples
Known GenesNFKB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572860
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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