A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5617760



Internal ID21566065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:25042007..25042007hg38UCSC Ensembl
chrX:25060124..25060124hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167131
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5617760
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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