A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561796



Internal ID20934867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22789338..22790036hg38UCSC Ensembl
chr7:22828957..22829655hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38699
hg19699
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272670
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561796
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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