A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103169



Internal ID21481383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14249474..14249474hg38UCSC Ensembl
chr19:14360286..14360286hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649126
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103169
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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