A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3943501



Internal ID21363570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14152003..14152003hg38UCSC Ensembl
chr6:14152234..14152234hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15201917
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3943501
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer