A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5599310



Internal ID21547944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2531342..2531658hg38UCSC Ensembl
chr20:2511988..2512304hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116274
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5599310
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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