A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025290



Internal ID21934633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85906185..85915095hg38UCSC Ensembl
chr15:86449416..86458326hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg388911
hg198911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598239
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025290
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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