A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1128716



Internal ID18902629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:21500195..21517688hg38UCSC Ensembl
Outerchr15:22143000..22160500hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3817494
hg1917501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960629
SamplesKWS1
Known GenesNF1P2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1128716
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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