A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17619712



Internal ID21811759
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 Variantsnsv6038446
Supporting Variants
Samples
Known GenesALOX15
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17619712
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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