A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17104557



Internal ID21458408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29839305..29839305hg38UCSC Ensembl
chr19:30330212..30330212hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381253
hg191253
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653430
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17104557
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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