A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767200



Internal ID20543060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77151710..77252848hg38UCSC Ensembl
chr3:77200861..77301999hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38101139
hg19101139
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272723
Samples
Known GenesROBO2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767200
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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