A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667554



Internal ID21615859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101842234..101842704hg38UCSC Ensembl
chrX:101097206..101097676hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17164993
SamplesHG01596
Known GenesNXF5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667554
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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