A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272376



Internal ID20839416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135978814..136004461hg38UCSC Ensembl
chr6:136299952..136325599hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3825648
hg1925648
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570790
Supporting Variants
Samples
Known GenesPDE7B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272376
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0008


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