A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832639



Internal ID22607574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38334034..38356835hg38UCSC Ensembl
chr2:38561176..38583977hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg3822802
hg1922802
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484832
Samples
Known GenesATL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832639
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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