A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14340509



Internal ID22280404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33462006..33470934hg38UCSC Ensembl
chr8:33319524..33328452hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg388929
hg198929
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3213477
Supporting Variants
SamplesNA19239
Known GenesFUT10
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14340509
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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