A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569893



Internal ID20942964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142327329..142403731hg38UCSC Ensembl
chr8:143408690..143485092hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3876403
hg1976403
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277289
Samples
Known GenesTSNARE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569893
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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