A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947536



Internal ID22723042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39637402..39637504hg38UCSC Ensembl
chr19:40128042..40128144hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389928
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947536
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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