A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111936



Internal ID18907518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:13200608..13202637hg38UCSC Ensembl
Outerchr16:13294465..13296494hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg382030
hg192030
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1300n106
Supporting Variantsnssv3964852
SamplesKWS2
Known GenesSHISA9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111936
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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