A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760547



Internal ID20536407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:46651273..46669427hg38UCSC Ensembl
chr7:46690871..46709025hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3818155
hg1918155
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274040
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760547
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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