A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115439



Internal ID19270600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:117126395..117129595hg38UCSC Ensembl
Outerchr12:117564200..117567400hg19UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg383201
hg193201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv878n106
Supporting Variantsnssv3976493
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115439
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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