A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869143



Internal ID22644078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11972149..11977613hg38UCSC Ensembl
chr17:11875466..11880930hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg385465
hg195465
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480352, nssv17475404
Samples
Known GenesZNF18
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869143
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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