A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267798



Internal ID20477016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72320352..72320409hg38UCSC Ensembl
chr17:70316493..70316550hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736259
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267798
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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