A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086597



Internal ID21995830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124094027..124094027hg38UCSC Ensembl
chr11:123964734..123964734hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598731
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086597
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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