A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17104253



Internal ID21488505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29537703..29537703hg38UCSC Ensembl
chr19:30028610..30028610hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661762
Supporting Variants
SamplesNA18939
Known GenesVSTM2B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17104253
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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