A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526477



Internal ID22395857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43100111..43100197hg38UCSC Ensembl
chr3:43141603..43141689hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14306793, nssv14306792
SamplesNA19239, NA19240
Known GenesPOMGNT2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526477
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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