A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14346386



Internal ID22253746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34904710..34904797hg38UCSC Ensembl
chr9:34904707..34904794hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3228452
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14346386
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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