A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17358899



Internal ID22584568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103981010..103985728hg38UCSC Ensembl
chr11:103851738..103856456hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg384719
hg194719
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910718
Supporting Variants
Samples
Known GenesPDGFD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17358899
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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