A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373999



Internal ID22599668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44984150..45064699hg38UCSC Ensembl
chr15:45276348..45356897hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3880550
hg1980550
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971292
Supporting Variants
Samples
Known GenesSORD
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373999
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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