A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281723



Internal ID20490941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:111805544..111805834hg38UCSC Ensembl
chr3:111524391..111524681hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743689
Supporting Variants
Samples
Known GenesPHLDB2, PLCXD2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281723
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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