A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598566



Internal ID20971637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:79160858..79161704hg38UCSC Ensembl
chr18:76920858..76921704hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38847
hg19847
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244855
Samples
Known GenesATP9B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598566
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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