A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835252



Internal ID22610187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143500780..143502414hg38UCSC Ensembl
chr3:143219622..143221256hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg381635
hg191635
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485205
Samples
Known GenesSLC9A9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835252
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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