A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464041



Internal ID21121594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112537333..112537654hg38UCSC Ensembl
chr11:112408056..112408377hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986808
Samples
Known GenesLOC387810
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464041
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