A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665952



Internal ID21614257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:142351552..142351617hg38UCSC Ensembl
chrX:141439338..141439403hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165866
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665952
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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