A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558442



Internal ID20931513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:129862499..129863334hg38UCSC Ensembl
chr8:130874745..130875580hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38836
hg19836
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276252
Samples
Known GenesFAM49B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558442
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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