A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835044



Internal ID22609979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155839436..155849569hg38UCSC Ensembl
chr3:155557225..155567358hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3810134
hg1910134
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486461
Samples
Known GenesSLC33A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835044
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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