A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463627



Internal ID21121180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102459620..102465675hg38UCSC Ensembl
chr11:102330351..102336406hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg386056
hg196056
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985479
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463627
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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