A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034962



Internal ID21944305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102906059..102909881hg38UCSC Ensembl
chr11:102776789..102780611hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg383823
hg193823
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596219
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034962
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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