A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3953751



Internal ID21373820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38855590..38855639hg38UCSC Ensembl
chr19:39346230..39346279hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15176958
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3953751
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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