A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5672104



Internal ID21620409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:144761753..144762059hg38UCSC Ensembl
chrX:143843274..143843580hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166441
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5672104
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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