A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029119



Internal ID21938462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46737525..46738079hg38UCSC Ensembl
chr11:46759075..46759629hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38555
hg19555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595080
Samples
Known GenesF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029119
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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