A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17104478



Internal ID21459730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34818077..34818794hg38UCSC Ensembl
chr19:35308981..35309698hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38718
hg19718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591399
Supporting Variants
SamplesHG02818
Known GenesLOC400685
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17104478
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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