A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283576



Internal ID20492794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96328364..96328420hg38UCSC Ensembl
chr5:95664068..95664124hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742344
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283576
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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