A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3216806



Internal ID22362678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84655658..84655955hg38UCSC Ensembl
chr16:84689264..84689561hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14382288, nssv14382865, nssv14379671, nssv14376491, nssv14386069, nssv14384590, nssv14381786, nssv14377200
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, HG00733, HG00513, HG00514
Known GenesKLHL36
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3216806
Frequency
Sample Size9
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer