A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025771



Internal ID21935114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64280045..64280280hg38UCSC Ensembl
chr11:64047517..64047752hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590436
Samples
Known GenesBAD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025771
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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