A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767897



Internal ID20543757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69220539..69274690hg38UCSC Ensembl
chr4:70086257..70140408hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3854152
hg1954152
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265149
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767897
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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