A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038399



Internal ID21947742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99199645..99199705hg38UCSC Ensembl
chr14:99665982..99666042hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611765
Samples
Known GenesBCL11B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038399
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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