A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071160



Internal ID19324198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15651125..15651618hg38UCSC Ensembl
chr19:15761935..15762428hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38494
hg19494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769694
SamplesKWP1
Known GenesCYP4F3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071160
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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