A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274575



Internal ID20841615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:51105845..51107190hg38UCSC Ensembl
chr7:51173542..51174887hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg381346
hg191346
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571868
Supporting Variants
Samples
Known GenesCOBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274575
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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