A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125520



Internal ID19256342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:3663080..3663158hg38UCSC Ensembl
Outerchr11:3684310..3684388hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv577n106
Supporting Variantsnssv3983696
SamplesKWS2
Known GenesART1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125520
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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