A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033936



Internal ID21943279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134092289..134092348hg38UCSC Ensembl
chr11:133962184..133962243hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616520
Samples
Known GenesJAM3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033936
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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