A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17353788



Internal ID22579457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98448845..98452143hg38UCSC Ensembl
chr12:98842623..98845921hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg383299
hg193299
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973198
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17353788
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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