A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970107



Internal ID22745042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11146465..11146465hg38UCSC Ensembl
chr19:11257141..11257141hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409501
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970107
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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