A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036229



Internal ID21945572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96056551..96056661hg38UCSC Ensembl
chr11:95789715..95789825hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593102
Samples
Known GenesMAML2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036229
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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