A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5654965



Internal ID21603270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33215583..33215583hg38UCSC Ensembl
chr19:33706489..33706489hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104599
SamplesHG00732
Known GenesSLC7A10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5654965
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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