A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568859



Internal ID20941930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:101995465..102278614hg38UCSC Ensembl
chr4:102916622..103199771hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38283150
hg19283150
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263380
Samples
Known GenesBANK1, SLC39A8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568859
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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