A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087885



Internal ID21997118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37076089..37076089hg38UCSC Ensembl
chr11:37097639..37097639hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589141
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087885
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer