A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590229



Internal ID21538798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13368822..13368885hg38UCSC Ensembl
chr17:13272139..13272202hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087060
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590229
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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