A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071938



Internal ID18970678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49590942..49591743hg38UCSC Ensembl
chr19:50094199..50095000hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772060
SamplesKWP1
Known GenesPRR12, PRRG2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071938
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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