A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034413



Internal ID21943756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59690048..59690864hg38UCSC Ensembl
chr15:59982247..59983063hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612030
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034413
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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