A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091836



Internal ID22001069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45738075..45738075hg38UCSC Ensembl
chr11:45759626..45759626hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593953
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091836
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