A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558085



Internal ID331160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:57485588..57485639hg38UCSC Ensembl
chrX:57512021..57512072hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740308
Samples
Known GenesFAAH2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558085
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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