A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910718



Internal ID22685929
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 StatusM
Merged Variants
Supporting Variantsnssv17358899
Samples
Known GenesPDGFD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910718
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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