A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129510



Internal ID19283985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:7491543..7491765hg38UCSC Ensembl
Outerchr11:7512774..7512996hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3963744
SamplesKWS1
Known GenesOLFML1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129510
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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