A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526653



Internal ID22396035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86767545..86767606hg38UCSC Ensembl
chr3:86816695..86816756hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14307865, nssv14307864
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526653
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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