A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14305968



Internal ID22139135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36879550..36879774hg38UCSC Ensembl
chr3:36921041..36921265hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3205315
Supporting Variants
SamplesHG00513
Known GenesTRANK1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14305968
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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