A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071541



Internal ID19325959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46293519..46293864hg38UCSC Ensembl
chr19:46796776..46797121hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768529
SamplesKWP1
Known GenesRNU6-66P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071541
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer