A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668608



Internal ID21616913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:148016096..148016240hg38UCSC Ensembl
chrX:147097616..147097760hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166474
SamplesHG03125
Known GenesFMR1NB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668608
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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