A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874551



Internal ID22649503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:14186364..14187779hg38UCSC Ensembl
chr17:14089681..14091096hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg381416
hg191416
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475441
Samples
Known GenesCOX10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874551
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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