A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271718



Internal ID20480936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4640471..4641294hg38UCSC Ensembl
chr17:4543766..4544589hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38824
hg19824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744015
Supporting Variants
Samples
Known GenesALOX15
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271718
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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