A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573922



Internal ID20946993
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 StatusM
Merged Variantsdgv6882n223
Supporting Variantsnssv18274279
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573922
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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