A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16273342



Internal ID20482560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65080018..65080078hg38UCSC Ensembl
chr17:63076136..63076196hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735109
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16273342
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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