A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036729



Internal ID21946072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124693188..124701710hg38UCSC Ensembl
chr11:124563084..124571606hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg388523
hg198523
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609487
Samples
Known GenesSPA17
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036729
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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