A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5395606



Internal ID175029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22883659..22883710hg38UCSC Ensembl
chr1:23210152..23210203hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16900101
Samples
Known GenesEPHB2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5395606
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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