A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3195417



Internal ID22345604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107901922..107902058hg38UCSC Ensembl
chr7:107542367..107542503hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14337534
SamplesNA19239
Known GenesDLD
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3195417
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