A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563397



Internal ID336331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:310531..345591hg38UCSC Ensembl
chr7:350497..385557hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3835061
hg1935061
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16992062
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563397
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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