A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666602



Internal ID21614907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154831507..154831781hg38UCSC Ensembl
chrX:154059782..154060056hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166300
SamplesNA19239
Known GenesSMIM9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666602
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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