A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192191



Internal ID22342806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:122597909..122598057hg38UCSC Ensembl
chr4:123519064..123519212hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14317114
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192191
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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