A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025632



Internal ID21934975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111447131..111448399hg38UCSC Ensembl
chr11:111317856..111319124hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg381269
hg191269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616683
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025632
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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