A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941820



Internal ID22717251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39850080..39850651hg38UCSC Ensembl
chr17:38006333..38006904hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375331
Samples
Known GenesIKZF3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941820
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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