A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766372



Internal ID20542232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67180407..72632516hg38UCSC Ensembl
chr7:66645394..72097501hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg385452110
hg195452108
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270895
Samples
Known GenesAUTS2, CALN1, LOC100507468, LOC101929736, MIR3914-1, MIR3914-2, PMS2P4, STAG3L4, TYW1, TYW1B, WBSCR17
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766372
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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