A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199519



Internal ID22349090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88327672..88328616hg38UCSC Ensembl
chr4:89248824..89249768hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38945
hg19945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14316622, nssv14316623
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199519
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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