A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836151



Internal ID22611086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27671736..27677207hg38UCSC Ensembl
chr3:27713227..27718698hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg385472
hg195472
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490613
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836151
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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