A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657635



Internal ID21605940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35809804..35809804hg38UCSC Ensembl
chr19:36300706..36300706hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104616
SamplesNA19238
Known GenesPRODH2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657635
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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