A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584997



Internal ID21533541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26710086..26713223hg38UCSC Ensembl
chr10:26999015..27002152hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383138
hg193138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068217
SamplesHG00731
Known GenesPDSS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584997
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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