A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670508



Internal ID21618813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115458685..115458736hg38UCSC Ensembl
chrX:114693406..114693452hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3852
hg1947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17164757
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670508
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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