A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668286



Internal ID21616591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3383132..3383370hg38UCSC Ensembl
chrX:3301173..3301411hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167248
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668286
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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