A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024720



Internal ID21934063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41807272..41807601hg38UCSC Ensembl
chr11:41828822..41829151hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595509
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024720
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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