A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5542228



Internal ID316668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207196925..207196976hg38UCSC Ensembl
chr2:208061649..208061700hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16924747
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5542228
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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