A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273776



Internal ID20840816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15599679..15599783hg38UCSC Ensembl
chr7:15639304..15639408hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565595
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273776
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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