A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563587



Internal ID20936658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18075013..18524799hg38UCSC Ensembl
chr8:17932522..18382309hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38449787
hg19449788
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277400
Samples
Known GenesASAH1, NAT1, NAT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563587
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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