A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980020



Internal ID22754955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11817694..11825641hg38UCSC Ensembl
chr18:11817693..11825640hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg387948
hg197948
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382457
Samples
Known GenesGNAL
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5980020
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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