A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616166



Internal ID21564471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:144923018..144923018hg38UCSC Ensembl
chrX:144004538..144004538hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166444
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616166
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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