A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625736



Internal ID15502583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:133354210..133355038hg38UCSC Ensembl
Outerchr11:133224105..133224933hg19UCSC Ensembl
Outerchr11:132729315..132730143hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381097
hg191097
hg181097
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513344
Supporting Variants
Samples1
Known GenesOPCML
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625736
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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