A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14346227



Internal ID22255726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74129800..74132022hg38UCSC Ensembl
chr9:76744716..76746938hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382223
hg192223
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3224235
Supporting Variants
SamplesNA19238
Known GenesMIR6130
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14346227
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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