A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274279



Internal ID20841319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66179384..66181261hg38UCSC Ensembl
chr7:65644371..65646248hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg381878
hg191878
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573922
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274279
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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