A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566622



Internal ID20939693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13441627..15436149hg38UCSC Ensembl
chr8:13299136..15293658hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381994523
hg191994523
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277171
Samples
Known GenesC8orf48, DLC1, MIR383, SGCZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566622
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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