A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752719



Internal ID20528579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44854527..45034654hg38UCSC Ensembl
chr15:45146725..45326852hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38180128
hg19180128
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv36n199
Supporting Variantsnssv16261684
Samples
Known GenesC15orf43, SORD
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752719
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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