A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14348276



Internal ID22288421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107642086..107642269hg38UCSC Ensembl
chr9:110404367..110404550hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527098
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14348276
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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