A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222882



Internal ID22366814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32096381..32096619hg38UCSC Ensembl
chr12:32249315..32249553hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14363184, nssv14363183
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222882
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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