A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878091



Internal ID22653056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:22235178..22241948hg38UCSC Ensembl
chr2:22458050..22464820hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg386771
hg196771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17408119
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878091
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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