A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14326793



Internal ID22276260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24878884..24879196hg38UCSC Ensembl
chr6:24879112..24879424hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529337
Supporting Variants
SamplesNA19239
Known GenesFAM65B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14326793
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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