A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199829



Internal ID22349366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:54040760..54041074hg38UCSC Ensembl
chr4:54906927..54907241hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14312894, nssv14312895, nssv14312896
SamplesNA19238, HG00732, HG00513
Known GenesCHIC2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199829
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer