A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17629107



Internal ID21821154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4955813..4955890hg38UCSC Ensembl
chr17:4859108..4859185hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032091
Supporting Variants
Samples
Known GenesENO3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17629107
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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