A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5551475



Internal ID324927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41262226..41262235hg38UCSC Ensembl
chrX:41121479..41121488hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736556
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5551475
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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