A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14391337



Internal ID22211325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12361948..12361948hg38UCSC Ensembl
chr16:12455805..12455805hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3560597
Supporting Variants
SamplesHG00732
Known GenesSNX29
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14391337
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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