A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272584



Internal ID20839624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134671587..134672717hg38UCSC Ensembl
chr7:134356339..134357469hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381131
hg191131
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567513
Supporting Variants
Samples
Known GenesBPGM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272584
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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