A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214132



Internal ID22360877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10001..10519hg38UCSC Ensembl
chr16:60001..60519hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14372966, nssv14389810
SamplesHG00731, HG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214132
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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