A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274349



Internal ID20841389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137891867..137892660hg38UCSC Ensembl
chr7:137576613..137577406hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38794
hg19794
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559821
Supporting Variants
Samples
Known GenesCREB3L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274349
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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