A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835255



Internal ID22610190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:144204483..144210234hg38UCSC Ensembl
chr3:143923325..143929076hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg385752
hg195752
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485212
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835255
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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