A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5598013



Internal ID21546634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32238779..32238846hg38UCSC Ensembl
chr17:30565798..30565865hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081769
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5598013
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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