A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526030



Internal ID22395409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:10667741..10667842hg38UCSC Ensembl
chr4:10669365..10669466hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14312144
SamplesHG00514
Known GenesCLNK
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526030
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