A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14349083



Internal ID22261053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112791905..112797462hg38UCSC Ensembl
chr9:115554185..115559742hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg385558
hg195558
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3228861
Supporting Variants
SamplesNA19238
Known GenesSNX30
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14349083
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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