A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276633



Internal ID20843673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77659924..77660698hg38UCSC Ensembl
chr7:77289241..77290015hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564016
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276633
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00029


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