A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969162



Internal ID22744097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55170873..55170873hg38UCSC Ensembl
chr19:55682241..55682241hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17400827
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969162
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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