A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029502



Internal ID21938845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31312682..31313013hg38UCSC Ensembl
chr15:31604885..31605216hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600120
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029502
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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