A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3927979



Internal ID21348048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154850279..154850279hg38UCSC Ensembl
chr4:155771431..155771431hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15201257
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3927979
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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