A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943841



Internal ID22719296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11194421..11199658hg38UCSC Ensembl
chr17:11097738..11102975hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg385238
hg195238
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370964
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943841
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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