A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560906



Internal ID333900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:134786171..134786222hg38UCSC Ensembl
chrX:133920201..133920252hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg386018
hg196018
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742446
Samples
Known GenesFAM122B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560906
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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