A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587008



Internal ID21535566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:57293709..57294029hg38UCSC Ensembl
chr10:59053469..59053789hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071022
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587008
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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