A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025143



Internal ID21934486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87815584..87815718hg38UCSC Ensembl
chr11:87526476..87526610hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597328
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025143
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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