A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14353280



Internal ID22293127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74176014..74177663hg38UCSC Ensembl
chr10:75935772..75937421hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381650
hg191650
Variant TypeCNV duplication
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3217166
Supporting Variants
SamplesNA19240
Known GenesADK
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14353280
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