A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591970



Internal ID21540548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128209288..128209338hg38UCSC Ensembl
chr10:130007552..130007602hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068709
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591970
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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