A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14336537



Internal ID22308065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:69536042..69536491hg38UCSC Ensembl
chr7:69001028..69001477hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206962
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14336537
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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