A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152913



Internal ID18854208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:14893042..14911343hg38UCSC Ensembl
Outerchr16:14986899..15005200hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3818302
hg1918302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997949
SamplesKWB1
Known GenesMIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, NOMO1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152913
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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