A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560081



Internal ID333095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154839751..154839802hg38UCSC Ensembl
chrX:154068026..154068077hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738156
Samples
Known GenesF8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560081
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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