A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14348436



Internal ID22278441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128395662..128395849hg38UCSC Ensembl
chr9:131157941..131158128hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3213007
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14348436
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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