A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670663



Internal ID21618968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:138282589..138283031hg38UCSC Ensembl
chrX:137364748..137365190hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165741
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670663
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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