A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765331



Internal ID20541191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36695201..36695201hg38UCSC Ensembl
chr15:36987402..36987402hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282448
Samples
Known GenesC15orf41
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765331
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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