A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190889



Internal ID22341681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2852715..2853126hg38UCSC Ensembl
chr4:2854442..2854853hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14309892, nssv14309890, nssv14309891
SamplesNA19238, NA19239, NA19240
Known GenesADD1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3190889
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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