A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071891



Internal ID19326614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3029201..3029602hg38UCSC Ensembl
chr19:3029199..3029600hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768903
SamplesKWP1
Known GenesTLE2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071891
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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