A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565468



Internal ID20938539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30617751..30619145hg38UCSC Ensembl
chr8:30475268..30476662hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381395
hg191395
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277697
Samples
Known GenesGTF2E2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565468
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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