A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14345486



Internal ID22261422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18942027..18942109hg38UCSC Ensembl
chr9:18942025..18942107hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529432
Supporting Variants
SamplesNA19238
Known GenesFAM154A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14345486
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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