A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668866



Internal ID21617171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71520430..71521262hg38UCSC Ensembl
chrX:70740280..70741112hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38833
hg19833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167738
SamplesHG00731
Known GenesBCYRN1, TAF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668866
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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