A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600930



Internal ID21549573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94152031..94152119hg38UCSC Ensembl
chr11:93885197..93885285hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076660
SamplesNA19239
Known GenesPANX1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600930
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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