A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968608



Internal ID22743543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13935448..13965042hg38UCSC Ensembl
chr9:13935447..13965041hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3829595
hg1929595
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432866
Samples
Known GenesLINC00583
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968608
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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