A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5603110



Internal ID21551772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35406100..35410256hg38UCSC Ensembl
chr10:35695028..35699184hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg384157
hg194157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17069806
SamplesNA19983
Known GenesCCNY
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5603110
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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