A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3926340



Internal ID21346411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7752960..7752960hg38UCSC Ensembl
chr4:7754687..7754687hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15190596
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3926340
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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