A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834612



Internal ID22609547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:135768701..135791840hg38UCSC Ensembl
chr3:135487543..135510682hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3823140
hg1923140
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485103
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834612
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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