A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973620



Internal ID22748555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8363564..8363564hg38UCSC Ensembl
chr19:8428448..8428448hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396506
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973620
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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