A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14356337



Internal ID22142288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19507937..19508769hg38UCSC Ensembl
chr1:19834431..19835263hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38833
hg19833
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3194345
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14356337
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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