A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071935



Internal ID18970778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44747642..44749443hg38UCSC Ensembl
chr19:45250899..45252700hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg381802
hg191802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765011
SamplesKWP1
Known GenesBCL3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071935
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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