A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14346028



Internal ID22310277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42538712..42539011hg38UCSC Ensembl
chr9:44215178..44215449hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38300
hg19272
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3226067
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14346028
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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