A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832926



Internal ID22607861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25994460..25998419hg38UCSC Ensembl
chr2:26217329..26221288hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg383960
hg193960
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484065
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832926
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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