A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267332



Internal ID20476550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43578216..43578268hg38UCSC Ensembl
chr5:43578318..43578370hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746827
Supporting Variants
Samples
Known GenesNNT-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267332
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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