A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284915



Internal ID20494133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:59574025..59574092hg38UCSC Ensembl
chr5:58869851..58869918hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746464
Supporting Variants
Samples
Known GenesPDE4D
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284915
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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