A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667480



Internal ID21615785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:132610869..132611294hg38UCSC Ensembl
chrX:131744897..131745322hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg38426
hg19426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165695
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667480
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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