A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837200



Internal ID22612135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87143484..87152483hg38UCSC Ensembl
chr3:87192634..87201633hg19UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg389000
hg199000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496153
Samples
Known GenesLINC00506
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837200
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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