A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669560



Internal ID21617865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:8504173..8506324hg38UCSC Ensembl
chrX:8472214..8474365hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg382152
hg192152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17168901
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669560
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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