A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290849



Internal ID20500067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112150831..112150935hg38UCSC Ensembl
chr13:112805145..112805249hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734690
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290849
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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