A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569023



Internal ID20942094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33413647..33424130hg38UCSC Ensembl
chr8:33271165..33281648hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3810484
hg1910484
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277792
Samples
Known GenesFUT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569023
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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