A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16273437



Internal ID20482655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16127185..16127336hg38UCSC Ensembl
chr17:16030499..16030650hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4748839
Supporting Variants
Samples
Known GenesNCOR1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16273437
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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