A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879897



Internal ID22654867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:12067473..12067528hg38UCSC Ensembl
chr2:12207599..12207654hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402247
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879897
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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