A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1142130



Internal ID19255542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:122836537..122836614hg38UCSC Ensembl
Outerchr11:122707245..122707322hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3988029, nssv3993633
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1142130
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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