A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106473



Internal ID21498600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57266243..57268422hg38UCSC Ensembl
chr19:57777611..57779790hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg382180
hg192180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5595852
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106473
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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