A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614276



Internal ID21562581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:147892220..147892220hg38UCSC Ensembl
chrX:146973738..146973738hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166469
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614276
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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