A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1142862



Internal ID19286821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:39380382..39399404hg38UCSC Ensembl
Outerchr15:39672583..39691605hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3819023
hg1919023
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3979633
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1142862
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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