A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863809



Internal ID22638744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46875917..46888675hg38UCSC Ensembl
chr13:47450052..47462810hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3812759
hg1912759
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458836
Samples
Known GenesHTR2A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863809
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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