A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564407



Internal ID22433137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108644853..108644853hg38UCSC Ensembl
chr7:108285297..108285297hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14337566
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3564407
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