A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951071



Internal ID16953258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:112964879..112968078hg38UCSC Ensembl
Outerchr11:112835601..112838800hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999618
SamplesBILGI_BIOE
Known GenesNCAM1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951071
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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