A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1123058



Internal ID19278772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:63408519..63408849hg38UCSC Ensembl
Outerchr16:63442423..63442753hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3954841, nssv3991035
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1123058
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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