A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5598595



Internal ID21547222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:136404..136688hg38UCSC Ensembl
chr11:191879..192163hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096715
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5598595
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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