A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667454



Internal ID21615759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118031420..118031471hg38UCSC Ensembl
chrX:117165383..117165434hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165413
SamplesHG03065
Known GenesKLHL13
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667454
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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