A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665893



Internal ID21614198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42653036..42654617hg38UCSC Ensembl
chrX:42512288..42513869hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg381582
hg191582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167808
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665893
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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