A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036682



Internal ID21946025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39567282..39567417hg38UCSC Ensembl
chr15:39859483..39859618hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606680
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036682
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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