A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106384



Internal ID21488901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56807268..56810269hg38UCSC Ensembl
chr19:57318636..57321637hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg383002
hg193002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589556
Supporting Variants
SamplesNA18939
Known GenesPEG3, ZIM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106384
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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