A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037438



Internal ID21946781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118721982..118729207hg38UCSC Ensembl
chr11:118592691..118599916hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg387226
hg197226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611459
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037438
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