A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14335561



Internal ID22268502
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3209724
Supporting Variants
SamplesNA19238
Known GenesTECPR1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14335561
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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