A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566344



Internal ID20939415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15583163..15583905hg38UCSC Ensembl
chr9:15583161..15583903hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38743
hg19743
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280221
Samples
Known GenesCCDC171
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566344
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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