A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023627



Internal ID21932970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62953909..62958491hg38UCSC Ensembl
chr11:62721381..62725963hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg384583
hg194583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582812
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023627
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