A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277376



Internal ID20844416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17179403..17677131hg38UCSC Ensembl
chr8:17036912..17534640hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38497729
hg19497729
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573156
Supporting Variants
Samples
Known GenesCNOT7, MTMR7, MTUS1, PDGFRL, SLC7A2, VPS37A, ZDHHC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277376
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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