A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103408



Internal ID21428016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19326706..19326706hg38UCSC Ensembl
chr19:19437515..19437515hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664182
Supporting Variants
SamplesHG00731
Known GenesMAU2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103408
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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