A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087588



Internal ID21996821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31213132..31213132hg38UCSC Ensembl
chr11:31234679..31234679hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588138
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087588
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