A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16266395



Internal ID20475613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138143610..138143676hg38UCSC Ensembl
chr5:137479299..137479365hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746957
Supporting Variants
Samples
Known GenesBRD8
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16266395
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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