A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088592



Internal ID21997825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128495..128495hg38UCSC Ensembl
chr11:128495..128495hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589869
Samples
Known GenesLINC01001
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088592
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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