A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209724



Internal ID22357754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98225551..98245950hg38UCSC Ensembl
chr7:97854863..97875262hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3820400
hg1920400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14335563, nssv14335555, nssv14335562, nssv14335561, nssv14335558, nssv14335559, nssv14335557, nssv14335556, nssv14335560
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesTECPR1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3209724
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer