A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14334882



Internal ID22282464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16089460..16089460hg38UCSC Ensembl
chr7:16129085..16129085hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3565076
Supporting Variants
SamplesNA19239
Known GenesISPD
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14334882
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