A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590371



Internal ID21538940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15840063..15840374hg38UCSC Ensembl
chr17:15743377..15743688hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092202
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590371
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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