A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562631



Internal ID20935702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:43076188..43076604hg38UCSC Ensembl
chr8:42931331..42931747hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278090
Samples
Known GenesFNTA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562631
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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