A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573593



Internal ID20946664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28939024..28939792hg38UCSC Ensembl
chr8:28796541..28797309hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38769
hg19769
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277630
Samples
Known GenesHMBOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573593
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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