A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569582



Internal ID20942653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42979981..42981873hg38UCSC Ensembl
chr8:42835124..42837016hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg381893
hg191893
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278073
Samples
Known GenesHOOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569582
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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