A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3940140



Internal ID21360209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45277839..45277985hg38UCSC Ensembl
chr15:45570037..45570183hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15183801
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3940140
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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