A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259118



Internal ID20468306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38702591..38702649hg38UCSC Ensembl
chr13:39276728..39276786hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736701
Supporting Variants
Samples
Known GenesFREM2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259118
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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