A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556342



Internal ID329481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42733291..42739362hg38UCSC Ensembl
chr7:42772890..42778961hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg386072
hg196072
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16996296
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556342
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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