A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038884



Internal ID21948227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106000308..106000359hg38UCSC Ensembl
chr11:105871035..105871086hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584096
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038884
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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