A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665920



Internal ID21614225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107501344..107501532hg38UCSC Ensembl
chrX:106744574..106744762hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17164872
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665920
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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