A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980141



Internal ID22755076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:129885870..129959524hg38UCSC Ensembl
chr4:130807025..130880679hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg3873655
hg1973655
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419361
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5980141
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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