A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14305683



Internal ID22273852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18964581..18964862hg38UCSC Ensembl
chr3:19006073..19006354hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3526890
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14305683
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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