A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119421



Internal ID19257206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:86644313..86644367hg38UCSC Ensembl
Outerchr11:86355355..86355409hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959864
SamplesKWS1
Known GenesME3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119421
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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