A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573673



Internal ID20946744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145450333..145472371hg38UCSC Ensembl
chr7:145147426..145169464hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3822039
hg1922039
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275148
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573673
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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