A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276713



Internal ID20843753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81045473..81046688hg38UCSC Ensembl
chr7:80674789..80676004hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg381216
hg191216
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574067
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276713
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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