A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285071



Internal ID20494289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44857548..45031632hg38UCSC Ensembl
chr15:45149746..45323830hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38174085
hg19174085
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753087
Supporting Variants
Samples
Known GenesC15orf43, SORD
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285071
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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