A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106610



Internal ID21450654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57017501..57017662hg38UCSC Ensembl
chr19:57528869..57529030hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598528
Supporting Variants
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106610
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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