A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5431469



Internal ID210245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238295634..238296645hg38UCSC Ensembl
chr2:239204275..239205286hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg381012
hg191012
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16927087
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5431469
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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