A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17104511



Internal ID21493782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2761705..2761758hg38UCSC Ensembl
chr19:2761703..2761756hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601986
Supporting Variants
SamplesNA19238
Known GenesSGTA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17104511
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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