A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624803



Internal ID15848339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:63928746..63934253hg38UCSC Ensembl
Outerchr11:63696218..63701725hg19UCSC Ensembl
Outerchr11:63452794..63458301hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg385508
hg195508
hg185508
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512232
Supporting Variants
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624803
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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