A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618196



Internal ID21810243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5836344..5872476hg38UCSC Ensembl
chr17:5739664..5775796hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3836133
hg1936133
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6021641
Supporting Variants
Samples
Known GenesLOC339166
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618196
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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