A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743448



Internal ID20519436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44411814..44411881hg38UCSC Ensembl
chr13:44985950..44986017hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290148
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743448
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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