A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667415



Internal ID21615720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40661279..40661408hg38UCSC Ensembl
chrX:40520531..40520660hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167082
SamplesHG02587
Known GenesMED14
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667415
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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