A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14391438



Internal ID22306799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19706023..19710912hg38UCSC Ensembl
chr16:19717345..19722234hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg384890
hg194890
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3216679
Supporting Variants
SamplesNA19240
Known GenesKNOP1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14391438
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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