A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890261



Internal ID22665288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:181920908..181921205hg38UCSC Ensembl
chr2:182785635..182785932hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392859
Samples
Known GenesSSFA2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890261
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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