A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039379



Internal ID21948722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41293522..41293590hg38UCSC Ensembl
chr15:41585720..41585788hg19UCSC 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 Variantsnssv17612510
Samples
Known GenesOIP5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039379
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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