A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740729



Internal ID20516706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41311821..41312231hg38UCSC Ensembl
chr15:41604019..41604429hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292134
Samples
Known GenesOIP5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740729
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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