A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569689



Internal ID20942760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:69396188..69397537hg38UCSC Ensembl
chr7:68861174..68862523hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg381350
hg191350
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275047
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569689
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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