A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081985



Internal ID21991218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:30785054..30785054hg38UCSC Ensembl
chr11:30806601..30806601hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584479
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081985
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