A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869012



Internal ID22643947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19963616..19964717hg38UCSC Ensembl
chr17:19866929..19868030hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381102
hg191102
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476160
Samples
Known GenesAKAP10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869012
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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