A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864368



Internal ID22639303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:20604690..20624314hg38UCSC Ensembl
chr11:20626236..20645860hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3819625
hg1919625
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463555
Samples
Known GenesSLC6A5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864368
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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