A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587924



Internal ID21536484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70411185..70411234hg38UCSC Ensembl
chr11:70257291..70257340hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075518
SamplesHG03009
Known GenesCTTN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587924
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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