A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026600



Internal ID21935943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118330954..118331008hg38UCSC Ensembl
chr11:118201669..118201723hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606002
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026600
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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