A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3939293



Internal ID21359362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46776357..46776357hg38UCSC Ensembl
chr1:47242029..47242029hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15194217
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3939293
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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