A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849939



Internal ID22624874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:20630390..20632527hg38UCSC Ensembl
chr11:20651936..20654073hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382138
hg192138
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465039
Samples
Known GenesSLC6A5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849939
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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