A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5598041



Internal ID21546662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:136269..136371hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096066
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5598041
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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