A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881372



Internal ID22656347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3131056..3131169hg38UCSC Ensembl
chr2:3134828..3134941hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17407038
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881372
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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