A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831062



Internal ID22605997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10293374..10298902hg38UCSC Ensembl
chr2:10433500..10439028hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg385529
hg195529
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484896
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831062
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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