A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3951265



Internal ID21371334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168309407..168309407hg38UCSC Ensembl
chr6:168710087..168710087hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15203283
SamplesHG002
Known GenesDACT2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3951265
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