A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936817



Internal ID22712176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:55166591..55177025hg38UCSC Ensembl
chr17:53243952..53254386hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3810435
hg1910435
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386252
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936817
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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