A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5549445



Internal ID323106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19057796..19057796hg38UCSC Ensembl
chr11:19079343..19079343hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044699
Samples
Known GenesMRGPRX2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5549445
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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