A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979114



Internal ID22754049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87937547..87949082hg38UCSC Ensembl
chr4:88858699..88870234hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3811536
hg1911536
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416478
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979114
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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