A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026969



Internal ID21936312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65757788..65757859hg38UCSC Ensembl
chr11:65525259..65525330hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583637
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026969
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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