A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868496



Internal ID22643431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25041603..25041701hg38UCSC Ensembl
chr2:25264472..25264570hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398978
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868496
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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