A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141205



Internal ID18902961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:132322106..132327306hg38UCSC Ensembl
Outerchr11:132192000..132197200hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg385201
hg195201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3992711
SamplesKWS2
Known GenesNTM
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141205
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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