A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3929416



Internal ID21349486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55569962..55569962hg38UCSC Ensembl
chr5:54865790..54865790hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15201392
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3929416
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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