A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669139



Internal ID21617444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:100723965..100724014hg38UCSC Ensembl
chrX:99978946..99978995hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17164850
SamplesHG02011
Known GenesSYTL4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669139
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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