A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3953111



Internal ID21373181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45643100..45643100hg38UCSC Ensembl
chr6:45610837..45610837hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15202771
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3953111
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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