A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229976



Internal ID22371649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19665089..19665431hg38UCSC Ensembl
chr19:19775898..19776240hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14287283
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229976
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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