A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3938590



Internal ID21358661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:28247911..28248245hg38UCSC Ensembl
chr18:25827875..25828209hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15176617
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3938590
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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