A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833068



Internal ID22608003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:57908902..57914859hg38UCSC Ensembl
chr2:58136037..58141994hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg385958
hg195958
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487476
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833068
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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