A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572276



Internal ID20945347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28976943..28977740hg38UCSC Ensembl
chr8:28834460..28835257hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38798
hg19798
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277634
Samples
Known GenesHMBOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572276
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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