A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3945805



Internal ID21365874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20506345..20506845hg38UCSC Ensembl
chr14:20974504..20975004hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15183290
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3945805
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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