A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745842



Internal ID20521853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41293520..41293588hg38UCSC Ensembl
chr15:41585718..41585786hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293344
Samples
Known GenesOIP5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745842
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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