A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968287



Internal ID22743223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95978084..96008582hg38UCSC Ensembl
chr14:96444421..96474919hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3830499
hg1930499
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383255
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968287
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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