A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561352



Internal ID20934423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:109876298..109896704hg38UCSC Ensembl
chr7:109516355..109536761hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3820407
hg1920407
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273639
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561352
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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