A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441063



Internal ID22498933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114106457..114343345hg38UCSC Ensembl
chr9:116868737..117105625hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38236889
hg19236889
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970795
Supporting Variants
Samples
Known GenesAKNA, COL27A1, MIR455, ORM1, ORM2
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441063
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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