A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283477



Internal ID20492695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:35191044..35191380hg38UCSC Ensembl
chr5:35191146..35191482hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743883
Supporting Variants
Samples
Known GenesPRLR
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283477
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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