A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834727



Internal ID22609662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153881367..153896013hg38UCSC Ensembl
chr3:153599156..153613802hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3814647
hg1914647
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485736
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834727
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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