A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972251



Internal ID22747186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71857845..71921692hg38UCSC Ensembl
chr15:72150186..72214033hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3863848
hg1963848
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384924
Samples
Known GenesMYO9A
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972251
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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