A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073226



Internal ID19317327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:59139533..59139839hg38UCSC Ensembl
chr3:59125259..59125565hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768505
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073226
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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