A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283338



Internal ID20492556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:80401620..80403988hg38UCSC Ensembl
chr17:78375420..78377788hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg382369
hg192369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744712
Supporting Variants
Samples
Known GenesLOC100294362
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283338
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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