A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273596



Internal ID20840636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107636093..107636740hg38UCSC Ensembl
chr7:107276538..107277185hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38648
hg19648
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566837
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273596
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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