A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038659



Internal ID21948002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95483217..95483291hg38UCSC Ensembl
chr11:95216381..95216455hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594764
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038659
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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