A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3940857



Internal ID21360926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3293967..3293967hg38UCSC Ensembl
chr4:3295694..3295694hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15190207
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3940857
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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