A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17630909



Internal ID21822956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35491580..35505207hg38UCSC Ensembl
chr17:33818599..33832226hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3813628
hg1913628
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023524
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17630909
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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