A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17081769



Internal ID21490359
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 StatusS
Merged Variantsnsv5598013
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17081769
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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