A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613858



Internal ID21562163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:147912049..147912049hg38UCSC Ensembl
chrX:146993567..146993567hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166471
SamplesNA12329
Known GenesFMR1, FMR1-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613858
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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