A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5588117



Internal ID21536677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15773473..15785818hg38UCSC Ensembl
chr17:15676787..15689132hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3812346
hg1912346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095614
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5588117
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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