A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17443171



Internal ID22501041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15024886..15031177hg38UCSC Ensembl
chr9:15024884..15031175hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg386292
hg196292
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968010
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17443171
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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