A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972359



Internal ID22747294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11509271..11511469hg38UCSC Ensembl
chr18:11509270..11511468hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg382199
hg192199
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381387
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972359
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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