A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567444



Internal ID20940515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:10715675..10755089hg38UCSC Ensembl
chr9:10715675..10755089hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3839415
hg1939415
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279437
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567444
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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