A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3946089



Internal ID21366159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2972360..2972360hg38UCSC Ensembl
chr6:2972594..2972594hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15201882
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3946089
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