A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645403



Internal ID21593708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51392110..51392110hg38UCSC Ensembl
chr19:51895364..51895364hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17106043
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645403
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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