A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229988



Internal ID22371656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11789828..11790079hg38UCSC Ensembl
chr16:11883684..11883935hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14381035, nssv14388708, nssv14373391
SamplesHG00731, HG00732, HG00733
Known GenesZC3H7A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229988
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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