A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211669



Internal ID22359151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12292301..12294048hg38UCSC Ensembl
chr19:12403116..12404863hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381748
hg191748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14286008
SamplesHG00732
Known GenesZNF44
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211669
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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