A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1116762



Internal ID19262083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:24892502..24892596hg38UCSC Ensembl
Outerchr15:25137649..25137743hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1179n106
Supporting Variantsnssv3979325
SamplesKWS2
Known GenesSNRPN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1116762
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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