A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272660



Internal ID20481878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167297644..167303284hg38UCSC Ensembl
chr5:166724649..166730289hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg385641
hg195641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734143
Supporting Variants
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272660
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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