A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881132



Internal ID22656106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:108882895..108882982hg38UCSC Ensembl
chr2:109499351..109499438hg19UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17408837
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881132
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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