A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17421620



Internal ID22479490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184943379..184953892hg38UCSC Ensembl
chr4:185864533..185875046hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3810514
hg1910514
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5967786
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17421620
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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