A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036596



Internal ID21945939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10489510..10517568hg38UCSC Ensembl
chr11:10511057..10539115hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3828059
hg1928059
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577611
Samples
Known GenesAMPD3, MIR4485, MTRNR2L8, RNF141
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036596
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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