A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869943



Internal ID22644878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16077849..16078946hg38UCSC Ensembl
chr2:16217971..16219068hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg381098
hg191098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402089
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869943
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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