A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970114



Internal ID22745049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38726064..38755207hg38UCSC Ensembl
chr15:39018265..39047408hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3829144
hg1929144
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378513
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970114
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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