A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14379920



Internal ID22266556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34184306..34184460hg38UCSC Ensembl
chr15:34476507..34476661hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3227799
Supporting Variants
SamplesNA19238
Known GenesKATNBL1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14379920
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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